Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38403698C= , CM000685.2:g.38403698C= | GRCh38 |
| NC_000023.10:g.38262951C= , CM000685.1:g.38262951C= | GRCh37 |
| NC_000023.9:g.38147895C= | NCBI36 |
| NG_008471.1:g.56216C= |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.621C= MANE Select | NP_000522.3:p.Ser207= |
| ENST00000039007.5:c.621C= MANE Select | ENSP00000039007.4:p.Ser207= |
| NM_000531.5:c.621C= | NP_000522.3:p.Ser207= |
| ENST00000039007.4:c.621C= | ENSP00000039007.4:p.Ser207= |
| ENST00000465127.1:c.172-262423C= | ENSP00000417050.1:n.172-262423C= |
| ENST00000643344.1:c.*371C= | ENSP00000496606.1:n.*371C= |
| XM_017029556.1:c.621C= | XP_016885045.1:p.Ser207= |