Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.78780660A>T , CM000667.2:g.78780660A>T | GRCh38 |
| NC_000005.9:g.78076483A>T , CM000667.1:g.78076483A>T | GRCh37 |
| NC_000005.8:g.78112239A>T | NCBI36 |
| NG_007089.1:g.210875T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000046.5:c.1339T>A MANE Select | NP_000037.2:p.Cys447Ser |
| ENST00000264914.10:c.1339T>A MANE Select | ENSP00000264914.4:p.Cys447Ser |
| NM_000046.3:c.1339T>A | NP_000037.2:p.Cys447Ser |
| NM_000046.4:c.1339T>A | NP_000037.2:p.Cys447Ser |
| ENST00000264914.8:c.1339T>A | ENSP00000264914.4:p.Cys447Ser |
| ENST00000521011.1:n.304T>A | |
| XM_011543390.1:c.1339T>A | XP_011541692.1:p.Cys447Ser |