Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.46853738G>A , CM000685.2:g.46853738G>A | GRCh38 |
| NC_000023.10:g.46713173G>A , CM000685.1:g.46713173G>A | GRCh37 |
| NC_000023.9:g.46598117G>A | NCBI36 |
| NG_009107.1:g.21827G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006915.3:c.365G>A MANE Select | NP_008846.2:p.Cys122Tyr |
| ENST00000218340.4:c.365G>A MANE Select | ENSP00000218340.3:p.Cys122Tyr |
| NM_006915.2:c.365G>A | NP_008846.2:p.Cys122Tyr |
| ENST00000218340.3:c.365G>A | ENSP00000218340.3:p.Cys122Tyr |