Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000019.10:g.7533842C>A , CM000681.2:g.7533842C>A | GRCh38 |
| NC_000019.9:g.7598728C>A , CM000681.1:g.7598728C>A | GRCh37 |
| NC_000019.8:g.7504728C>A | NCBI36 |
| NG_013374.1:g.4691C>A | |
| NG_015806.1:g.16233C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264079.11:c.*47C>A MANE Select | ENSP00000264079.5:n.*47C>A | |
| ENST00000264079.10:c.*47C>A | ENSP00000264079.5:n.*47C>A | |
| ENST00000394321.9:n.2105C>A | ||
| ENST00000599334.1:c.518C>A | ||
| ENST00000601870.1:c.143C>A | ||
| ENST00000602227.1:n.344C>A | ||
| NM_020533.2:c.*47C>A | NP_065394.1:n.*47C>A | |
| NM_020533.3:c.*47C>A MANE Select | NP_065394.1:n.*47C>A |