Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68438962C>A , CM000663.2:g.68438962C>A | GRCh38 |
| NC_000001.10:g.68904645C>A , CM000663.1:g.68904645C>A | GRCh37 |
| NC_000001.9:g.68677233C>A | NCBI36 |
| NG_008472.1:g.15998G>T | |
| NG_008472.2:g.15998G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000329.3:c.978G>T MANE Select | NP_000320.1:p.Val326= |
| ENST00000262340.6:c.978G>T MANE Select | ENSP00000262340.5:p.Val326= |
| NM_000329.2:c.978G>T | NP_000320.1:p.Val326= |
| ENST00000262340.5:c.978G>T | ENSP00000262340.5:p.Val326= |
| XM_017002027.1:c.702G>T | XP_016857516.1:p.Val234= |