Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.102532471A>G , CM000664.2:g.102532471A>G | GRCh38 |
| NC_000002.11:g.103148930A>G , CM000664.1:g.103148930A>G | GRCh37 |
| NC_000002.10:g.102515362A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295269.5:c.2180A>G MANE Select | ENSP00000295269.4:p.Tyr727Cys | |
| ENST00000295269.4:c.2180A>G | ENSP00000295269.4:p.Tyr727Cys | |
| NM_001011552.3:c.2180A>G | NP_001011552.2:p.Tyr727Cys | |
| XM_011511158.1:c.2093A>G | XP_011509460.1:p.Tyr698Cys | |
| NM_001011552.4:c.2180A>G MANE Select | NP_001011552.2:p.Tyr727Cys |