Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38408922A= , CM000685.2:g.38408922A= | GRCh38 |
| NC_000023.10:g.38268175A= , CM000685.1:g.38268175A= | GRCh37 |
| NC_000023.9:g.38153119A= | NCBI36 |
| NG_008471.1:g.61440A= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.764A= MANE Select | NP_000522.3:p.His255= |
| ENST00000039007.5:c.764A= MANE Select | ENSP00000039007.4:p.His255= |
| NM_000531.5:c.764A= | NP_000522.3:p.His255= |
| ENST00000039007.4:c.764A= | ENSP00000039007.4:p.His255= |
| ENST00000465127.1:c.172-257199A= | ENSP00000417050.1:n.172-257199A= |
| ENST00000643344.1:c.*514A= | ENSP00000496606.1:n.*514A= |
| XM_017029556.1:c.764A= | XP_016885045.1:p.His255= |