Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.154571359A>G , CM000663.2:g.154571359A>G | GRCh38 |
| NC_000001.10:g.154543835A>G , CM000663.1:g.154543835A>G | GRCh37 |
| NC_000001.9:g.152810459A>G | NCBI36 |
| NG_008027.1:g.8579A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000368476.4:c.536A>G MANE Select | ENSP00000357461.3:p.Asp179Gly | |
| ENST00000636034.1:c.536A>G | ENSP00000489703.1:p.Asp179Gly | |
| ENST00000637900.1:c.542A>G | ENSP00000490474.1:p.Asp181Gly | |
| ENST00000368476.3:c.536A>G | ENSP00000357461.3:p.Asp179Gly | |
| NM_000748.2:c.536A>G | NP_000739.1:p.Asp179Gly | |
| XM_017000180.2:c.26A>G | XP_016855669.1:p.Asp9Gly | |
| XR_001736952.2:n.788A>G | ||
| NM_000748.3:c.536A>G MANE Select | NP_000739.1:p.Asp179Gly |