Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.46040928C>T , CM000666.2:g.46040928C>T | GRCh38 |
| NC_000004.11:g.46042945C>T , CM000666.1:g.46042945C>T | GRCh37 |
| NC_000004.10:g.45737702C>T | NCBI36 |
| NG_046964.1:g.88138G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_173536.4:c.*60G>A MANE Select | NP_775807.2:n.*60G>A |
| ENST00000295452.5:c.*60G>A MANE Select | ENSP00000295452.4:n.*60G>A |
| NM_173536.3:c.*60G>A | NP_775807.2:n.*60G>A |
| ENST00000295452.4:c.*60G>A | ENSP00000295452.4:n.*60G>A |
| XM_017007990.2:c.*60G>A | XP_016863479.1:n.*60G>A |