Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7522766G>T , CM000681.2:g.7522766G>T | GRCh38 |
| NC_000019.9:g.7587652G>T , CM000681.1:g.7587652G>T | GRCh37 |
| NC_000019.8:g.7493652G>T | NCBI36 |
| NG_015806.1:g.5157G>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.16G>T MANE Select | ENSP00000264079.5:p.Gly6Cys | |
| ENST00000264079.10:c.16G>T | ENSP00000264079.5:p.Gly6Cys | |
| ENST00000394321.9:n.96G>T | ||
| ENST00000596390.1:n.132G>T | ||
| ENST00000601003.1:c.16G>T | ENSP00000469074.1:p.Gly6Cys | |
| NM_020533.2:c.16G>T | NP_065394.1:p.Gly6Cys | |
| XR_936293.1:n.926+76C>A | ||
| XR_936294.1:n.926+76C>A | ||
| XR_936295.1:n.570+76C>A | ||
| XR_936293.2:n.952+76C>A | ||
| XR_936294.2:n.952+76C>A | ||
| NM_020533.3:c.16G>T MANE Select | NP_065394.1:p.Gly6Cys |