Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38403703C= , CM000685.2:g.38403703C= | GRCh38 |
| NC_000023.10:g.38262956C= , CM000685.1:g.38262956C= | GRCh37 |
| NC_000023.9:g.38147900C= | NCBI36 |
| NG_008471.1:g.56221C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.626C= MANE Select | NP_000522.3:p.Ala209= |
| ENST00000039007.5:c.626C= MANE Select | ENSP00000039007.4:p.Ala209= |
| NM_000531.5:c.626C= | NP_000522.3:p.Ala209= |
| ENST00000039007.4:c.626C= | ENSP00000039007.4:p.Ala209= |
| ENST00000465127.1:c.172-262418C= | ENSP00000417050.1:n.172-262418C= |
| ENST00000643344.1:c.*376C= | ENSP00000496606.1:n.*376C= |
| XM_017029556.1:c.626C= | XP_016885045.1:p.Ala209= |