Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.83285045T>C , CM000666.2:g.83285045T>C | GRCh38 |
| NC_000004.11:g.84206198T>C , CM000666.1:g.84206198T>C | GRCh37 |
| NC_000004.10:g.84425222T>C | NCBI36 |
| NG_015825.1:g.4870A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_015697.8:c.-131A>G | NP_056512.5:n.-131A>G |
| NM_015697.9:c.-131A>G | NP_056512.5:n.-131A>G |
| XM_011531855.1:c.-131A>G | XP_011530157.1:n.-131A>G |
| XM_011531856.1:c.-131A>G | XP_011530158.1:n.-131A>G |
| XM_011531857.1:c.-131A>G | XP_011530159.1:n.-131A>G |
| XM_011531858.1:c.-131A>G | XP_011530160.1:n.-131A>G |
| XM_011531859.1:c.-131A>G | XP_011530161.1:n.-131A>G |
| XM_011531860.1:c.-131A>G | XP_011530162.1:n.-131A>G |
| XM_011531861.1:c.-131A>G | XP_011530163.1:n.-131A>G |
| XM_011531862.1:c.-131A>G | XP_011530164.1:n.-131A>G |
| XM_011531863.1:c.-131A>G | XP_011530165.1:n.-131A>G |
| XM_011531864.1:c.-131A>G | XP_011530166.1:n.-131A>G |
| XM_011531865.1:c.-131A>G | XP_011530167.1:n.-131A>G |
| XM_011531866.1:c.-131A>G | XP_011530168.1:n.-131A>G |
| XR_427543.2:n.29A>G | |
| XR_938721.1:n.45A>G |