Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.11965482T= , CM000663.2:g.11965482T= | GRCh38 |
| NC_000001.10:g.12025539T= , CM000663.1:g.12025539T= | GRCh37 |
| NC_000001.9:g.11948126T= | NCBI36 |
| NG_008159.1:g.35794T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000196061.5:c.1473T= MANE Select | ENSP00000196061.4:p.Asp491= | |
| ENST00000196061.4:c.1473T= | ENSP00000196061.4:p.Asp491= | |
| ENST00000470133.1:n.87T= | ||
| ENST00000491536.5:n.101T= | ||
| NM_000302.3:c.1473T= | NP_000293.2:p.Asp491= | |
| NM_001316320.1:c.1614T= | NP_001303249.1:p.Asp538= | |
| XM_011541594.1:c.1554T= | XP_011539896.1:p.Asp518= | |
| XM_024447707.1:c.807T= | XP_024303475.1:p.Asp269= | |
| NM_000302.4:c.1473T= MANE Select | NP_000293.2:p.Asp491= | |
| NM_001316320.2:c.1614T= | NP_001303249.1:p.Asp538= |