Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38352782T>A , CM000685.2:g.38352782T>A | GRCh38 |
| NC_000023.10:g.38212035T>A , CM000685.1:g.38212035T>A | GRCh37 |
| NC_000023.9:g.38096979T>A | NCBI36 |
| NG_008471.1:g.5300T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000531.6:c.77+9T>A MANE Select | NP_000522.3:n.77+9T>A |
| ENST00000039007.5:c.77+9T>A MANE Select | ENSP00000039007.4:n.77+9T>A |
| NM_000531.5:c.77+9T>A | NP_000522.3:n.77+9T>A |
| ENST00000039007.4:c.77+9T>A | ENSP00000039007.4:n.77+9T>A |
| ENST00000465127.1:c.172-313339T>A | ENSP00000417050.1:n.172-313339T>A |
| ENST00000488812.1:n.169+9T>A | |
| ENST00000643344.1:c.77+9T>A | ENSP00000496606.1:n.77+9T>A |
| XM_017029556.1:c.77+9T>A | XP_016885045.1:n.77+9T>A |