Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.42403188C>T , CM000679.2:g.42403188C>T | GRCh38 |
| NC_000017.10:g.40555206C>T , CM000679.1:g.40555206C>T | GRCh37 |
| NC_000017.9:g.37808732C>T | NCBI36 |
| NG_015845.1:g.25133G>A | |
| NG_015845.2:g.25133G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357037.6:c.*1499G>A MANE Select | ENSP00000349541.4:n.*1499G>A | |
| ENST00000357037.5:c.*1499G>A | ENSP00000349541.4:n.*1499G>A | |
| NM_012232.5:c.*1499G>A | NP_036364.2:n.*1499G>A | |
| NM_012232.6:c.*1499G>A MANE Select | NP_036364.2:n.*1499G>A |