Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.19955894G>T , CM000670.2:g.19955894G>T | GRCh38 |
| NC_000008.10:g.19813405G>T , CM000670.1:g.19813405G>T | GRCh37 |
| NC_000008.9:g.19857685G>T | NCBI36 |
| NG_008855.1:g.21824G>T | |
| NG_008855.2:g.59178G>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000237.3:c.829G>T MANE Select | NP_000228.1:p.Asp277Tyr |
| ENST00000650287.1:c.829G>T MANE Select | ENSP00000497642.1:p.Asp277Tyr |
| NM_000237.2:c.829G>T | NP_000228.1:p.Asp277Tyr |
| ENST00000311322.8:c.829G>T | ENSP00000309757.6:p.Asp277Tyr |