Linked Data
ClinVar Variation Id:
1997180
dbSNP Id:
rs970542777
gnomAD v2:
16-68863586-C-A
gnomAD v4:
16-68829683-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68829683C>A , CM000678.2:g.68829683C>A | GRCh38 |
| NC_000016.9:g.68863586C>A , CM000678.1:g.68863586C>A | GRCh37 |
| NC_000016.8:g.67421087C>A | NCBI36 |
| NG_008021.1:g.97392C>A , LRG_301:g.97392C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.2325C>A MANE Select | ENSP00000261769.4:p.Gly775= | |
| ENST00000261769.9:c.2325C>A | ENSP00000261769.4:p.Gly775= | |
| ENST00000422392.6:c.2142C>A | ENSP00000414946.2:p.Gly714= | |
| ENST00000562118.1:n.543C>A | ||
| ENST00000562836.5:n.2396C>A | ||
| ENST00000566510.5:c.*991C>A | ENSP00000458139.1:n.*991C>A | |
| ENST00000566612.5:c.*565C>A | ENSP00000454782.1:n.*565C>A | |
| ENST00000611625.4:c.2388C>A | ENSP00000481063.1:p.Gly796= | |
| ENST00000612417.4:c.1853+3129C>A | ENSP00000478360.1:n.1853+3129C>A | |
| ENST00000621016.4:c.1866-4520C>A | ENSP00000480664.1:n.1866-4520C>A | |
| NM_004360.3:c.2325C>A , LRG_301t1:c.2325C>A | NP_004351.1:p.Gly775= | |
| XM_011523488.1:c.1590C>A | XP_011521790.1:p.Gly530= | |
| XM_011523489.1:c.1590C>A | XP_011521791.1:p.Gly530= | |
| NM_001317184.1:c.2142C>A | NP_001304113.1:p.Gly714= | |
| NM_001317185.1:c.777C>A | NP_001304114.1:p.Gly259= | |
| NM_001317186.1:c.360C>A | NP_001304115.1:p.Gly120= | |
| NM_004360.4:c.2325C>A | NP_004351.1:p.Gly775= | |
| NM_004360.5:c.2325C>A MANE Select | NP_004351.1:p.Gly775= | |
| NM_001317184.2:c.2142C>A | NP_001304113.1:p.Gly714= | |
| NM_001317185.2:c.777C>A | NP_001304114.1:p.Gly259= | |
| NM_001317186.2:c.360C>A | NP_001304115.1:p.Gly120= |