Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429880C= , CM000663.2:g.68429880C= | GRCh38 |
| NC_000001.10:g.68895563C= , CM000663.1:g.68895563C= | GRCh37 |
| NC_000001.9:g.68668151C= | NCBI36 |
| NG_008472.1:g.25080G= | |
| NG_008472.2:g.25080G= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1498G= MANE Select | ENSP00000262340.5:p.Ala500= | |
| ENST00000262340.5:c.1498G= | ENSP00000262340.5:p.Ala500= | |
| NM_000329.2:c.1498G= | NP_000320.1:p.Ala500= | |
| XM_017002027.1:c.1222G= | XP_016857516.1:p.Ala408= | |
| NM_000329.3:c.1498G= MANE Select | NP_000320.1:p.Ala500= |