Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.15239401C>T , CM000681.2:g.15239401C>T | GRCh38 |
| NC_000019.9:g.15350212C>T , CM000681.1:g.15350212C>T | GRCh37 |
| NC_000019.8:g.15211212C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000679869.1:c.3567G>A MANE Select | ENSP00000506350.1:p.Ala1189= | |
| ENST00000263377.6:c.3567G>A | ENSP00000263377.1:p.Ala1189= | |
| NM_058243.2:c.3567G>A | NP_490597.1:p.Ala1189= | |
| XM_011527854.1:c.3567G>A | XP_011526156.1:p.Ala1189= | |
| XM_011527854.2:c.3567G>A | XP_011526156.1:p.Ala1189= | |
| NM_001379291.1:c.3567G>A MANE Select | NP_001366220.1:p.Ala1189= | |
| NM_058243.3:c.3567G>A | NP_490597.1:p.Ala1189= |