Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.54999313G>A , CM000663.2:g.54999313G>A | GRCh38 |
| NC_000001.10:g.55464986G>A , CM000663.1:g.55464986G>A | GRCh37 |
| NC_000001.9:g.55237574G>A | NCBI36 |
| NG_008965.1:g.5370G>A | |
| NG_008965.2:g.5381G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_057176.3:c.127G>A MANE Select | NP_476517.1:p.Val43Ile |
| ENST00000651561.1:c.127G>A MANE Select | ENSP00000498282.1:p.Val43Ile |
| NM_057176.2:c.127G>A | NP_476517.1:p.Val43Ile |
| ENST00000371265.4:c.127G>A | ENSP00000360312.4:p.Val43Ile |