Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.9890802A>G , CM000665.2:g.9890802A>G | GRCh38 |
| NC_000003.11:g.9932486A>G , CM000665.1:g.9932486A>G | GRCh37 |
| NC_000003.10:g.9907486A>G | NCBI36 |
| NG_041779.1:g.5216A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000489724.2:c.80A>G | ENSP00000497724.1:p.Tyr27Cys | |
| ENST00000647897.1:c.80A>G MANE Select | ENSP00000496942.1:p.Tyr27Cys | |
| ENST00000307768.4:c.80A>G | ENSP00000306106.4:p.Tyr27Cys | |
| ENST00000489724.1:n.170A>G | ||
| ENST00000616966.2:c.80A>G | ENSP00000481606.1:p.Tyr27Cys | |
| NM_032492.3:c.80A>G | NP_115881.3:p.Tyr27Cys | |
| NM_001363890.1:c.-189A>G | NP_001350819.1:n.-189A>G | |
| NM_032492.4:c.80A>G MANE Select | NP_115881.3:p.Tyr27Cys |