Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.37974707G>T , CM000671.2:g.37974707G>T | GRCh38 |
| NC_000009.11:g.37974704G>T , CM000671.1:g.37974704G>T | GRCh37 |
| NC_000009.10:g.37964704G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377707.4:c.969C>A MANE Select | ENSP00000366936.3:p.Ser323Arg | |
| ENST00000377707.3:c.969C>A | ENSP00000366936.3:p.Ser323Arg | |
| ENST00000540557.1:c.*182C>A | ENSP00000457548.1:n.*182C>A | |
| NM_003028.2:c.969C>A | NP_003019.2:p.Ser323Arg | |
| NM_003028.3:c.969C>A MANE Select | NP_003019.2:p.Ser323Arg |