Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.78778762C>T , CM000667.2:g.78778762C>T | GRCh38 |
| NC_000005.9:g.78074585C>T , CM000667.1:g.78074585C>T | GRCh37 |
| NC_000005.8:g.78110341C>T | NCBI36 |
| NG_007089.1:g.212773G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000046.5:c.*1635G>A MANE Select | NP_000037.2:n.*1635G>A |
| ENST00000264914.10:c.*1635G>A MANE Select | ENSP00000264914.4:n.*1635G>A |
| NM_000046.3:c.*1635G>A | NP_000037.2:n.*1635G>A |
| NM_000046.4:c.*1635G>A | NP_000037.2:n.*1635G>A |
| ENST00000264914.8:c.*1635G>A | ENSP00000264914.4:n.*1635G>A |
| XM_011543390.1:c.*1635G>A | XP_011541692.1:n.*1635G>A |