Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.150986360A= , CM000663.2:g.150986360A= | GRCh38 |
| NC_000001.10:g.150958836A= , CM000663.1:g.150958836A= | GRCh37 |
| NC_000001.9:g.149225460A= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003568.3:c.497A= MANE Select | NP_003559.2:p.Asp166= |
| ENST00000368947.9:c.497A= MANE Select | ENSP00000357943.4:p.Asp166= |
| NM_003568.2:c.497A= | NP_003559.2:p.Asp166= |
| ENST00000368947.8:c.497A= | ENSP00000357943.4:p.Asp166= |
| XM_005245539.3:c.497A= | XP_005245596.1:p.Asp166= |
| XM_011510058.1:c.497A= | XP_011508360.1:p.Asp166= |
| XM_011510058.3:c.497A= | XP_011508360.1:p.Asp166= |