Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.153690466C>T , CM000685.2:g.153690466C>T | GRCh38 |
| NC_000023.10:g.152955921C>T , CM000685.1:g.152955921C>T | GRCh37 |
| NC_000023.9:g.152609115C>T | NCBI36 |
| NG_012016.1:g.7170C>T | |
| NG_012016.2:g.7170C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253122.10:c.354C>T MANE Select | ENSP00000253122.5:p.Ala118= | |
| ENST00000675713.1:n.108C>T | ||
| ENST00000253122.9:c.354C>T | ENSP00000253122.5:p.Ala118= | |
| ENST00000430077.6:c.9C>T | ENSP00000403041.2:p.Ala3= | |
| ENST00000476466.1:n.206C>T | ||
| NM_001142805.1:c.354C>T | NP_001136277.1:p.Ala118= | |
| NM_001142806.1:c.9C>T | NP_001136278.1:p.Ala3= | |
| NM_005629.3:c.354C>T | NP_005620.1:p.Ala118= | |
| NM_005629.4:c.354C>T MANE Select | NP_005620.1:p.Ala118= | |
| NM_001142805.2:c.354C>T | NP_001136277.1:p.Ala118= |