gnomAD v3:
gnomAD v4:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.71664965C>T , CM000664.2:g.71664965C>T | GRCh38 |
| NC_000002.11:g.71892095C>T , CM000664.1:g.71892095C>T | GRCh37 |
| NC_000002.10:g.71745603C>T | NCBI36 |
| NG_008694.1:g.216343C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000698057.1:c.2589-197C>T | ENSP00000513536.1:n.2589-197C>T | |
| ENST00000698058.1:c.1806-197C>T | ENSP00000513537.1:n.1806-197C>T | |
| ENST00000698059.1:c.1914-197C>T | ENSP00000513538.1:n.1914-197C>T | |
| ENST00000258104.8:c.5058-197C>T MANE Plus Clinical | ENSP00000258104.3:n.5058-197C>T | |
| ENST00000410020.8:c.5175-197C>T MANE Select | ENSP00000386881.3:n.5175-197C>T | |
| ENST00000258104.7:c.5058-197C>T | ENSP00000258104.3:n.5058-197C>T | |
| ENST00000394120.6:c.5061-197C>T | ENSP00000377678.2:n.5061-197C>T | |
| ENST00000409366.5:c.5124-197C>T | ENSP00000386512.1:n.5124-197C>T | |
| ENST00000409582.7:c.5172-197C>T | ENSP00000386547.3:n.5172-197C>T | |
| ENST00000409651.5:c.5154-197C>T | ENSP00000386683.1:n.5154-197C>T | |
| ENST00000409744.5:c.5082-197C>T | ENSP00000386285.1:n.5082-197C>T | |
| ENST00000409762.5:c.5109-197C>T | ENSP00000387137.1:n.5109-197C>T | |
| ENST00000410020.7:c.5175-197C>T | ENSP00000386881.3:n.5175-197C>T | |
| ENST00000410041.1:c.5112-197C>T | ENSP00000386617.1:n.5112-197C>T | |
| ENST00000413539.6:c.5151-197C>T | ENSP00000407046.2:n.5151-197C>T | |
| ENST00000429174.6:c.5121-197C>T | ENSP00000398305.2:n.5121-197C>T | |
| ENST00000479049.6:n.1943-197C>T | ||
| NM_001130455.1:c.5061-197C>T | NP_001123927.1:n.5061-197C>T | |
| NM_001130976.1:c.5016-197C>T | NP_001124448.1:n.5016-197C>T | |
| NM_001130977.1:c.5079-197C>T | NP_001124449.1:n.5079-197C>T | |
| NM_001130978.1:c.5121-197C>T | NP_001124450.1:n.5121-197C>T | |
| NM_001130979.1:c.5151-197C>T | NP_001124451.1:n.5151-197C>T | |
| NM_001130980.1:c.5109-197C>T | NP_001124452.1:n.5109-197C>T | |
| NM_001130981.1:c.5172-197C>T | NP_001124453.1:n.5172-197C>T | |
| NM_001130982.1:c.5154-197C>T | NP_001124454.1:n.5154-197C>T | |
| NM_001130983.1:c.5124-197C>T | NP_001124455.1:n.5124-197C>T | |
| NM_001130984.1:c.5082-197C>T | NP_001124456.1:n.5082-197C>T | |
| NM_001130985.1:c.5112-197C>T | NP_001124457.1:n.5112-197C>T | |
| NM_001130986.1:c.5019-197C>T | NP_001124458.1:n.5019-197C>T | |
| NM_001130987.1:c.5175-197C>T | NP_001124459.1:n.5175-197C>T | |
| NM_003494.3:c.5058-197C>T | NP_003485.1:n.5058-197C>T | |
| XM_005264584.3:c.5217-197C>T | XP_005264641.1:n.5217-197C>T | |
| XM_005264585.3:c.5214-197C>T | XP_005264642.1:n.5214-197C>T | |
| XM_005264584.4:c.5217-197C>T | XP_005264641.1:n.5217-197C>T | |
| XM_005264585.5:c.5214-197C>T | XP_005264642.1:n.5214-197C>T | |
| XR_001738969.1:n.5573-197C>T | ||
| NM_001130987.2:c.5175-197C>T MANE Select | NP_001124459.1:n.5175-197C>T | |
| NM_001130455.2:c.5061-197C>T | NP_001123927.1:n.5061-197C>T | |
| NM_001130976.2:c.5016-197C>T | NP_001124448.1:n.5016-197C>T | |
| NM_001130977.2:c.5079-197C>T | NP_001124449.1:n.5079-197C>T | |
| NM_001130978.2:c.5121-197C>T | NP_001124450.1:n.5121-197C>T | |
| NM_001130979.2:c.5151-197C>T | NP_001124451.1:n.5151-197C>T | |
| NM_001130980.2:c.5109-197C>T | NP_001124452.1:n.5109-197C>T | |
| NM_001130981.2:c.5172-197C>T | NP_001124453.1:n.5172-197C>T | |
| NM_001130982.2:c.5154-197C>T | NP_001124454.1:n.5154-197C>T | |
| NM_001130983.2:c.5124-197C>T | NP_001124455.1:n.5124-197C>T | |
| NM_001130984.2:c.5082-197C>T | NP_001124456.1:n.5082-197C>T | |
| NM_001130985.2:c.5112-197C>T | NP_001124457.1:n.5112-197C>T | |
| NM_001130986.2:c.5019-197C>T | NP_001124458.1:n.5019-197C>T | |
| NM_003494.4:c.5058-197C>T MANE Plus Clinical | NP_003485.1:n.5058-197C>T |