Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38421002C>A , CM000685.2:g.38421002C>A | GRCh38 |
| NC_000023.10:g.38280255C>A , CM000685.1:g.38280255C>A | GRCh37 |
| NC_000023.9:g.38165199C>A | NCBI36 |
| NG_008471.1:g.73520C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000039007.5:c.1006-21C>A MANE Select | ENSP00000039007.4:n.1006-21C>A | |
| ENST00000643344.1:c.*756-21C>A | ENSP00000496606.1:n.*756-21C>A | |
| ENST00000039007.4:c.1006-21C>A | ENSP00000039007.4:n.1006-21C>A | |
| ENST00000465127.1:c.172-245119C>A | ENSP00000417050.1:n.172-245119C>A | |
| NM_000531.5:c.1006-21C>A | NP_000522.3:n.1006-21C>A | |
| NM_000531.6:c.1006-21C>A MANE Select | NP_000522.3:n.1006-21C>A |