Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.8076322C>T , CM000679.2:g.8076322C>T | GRCh38 |
| NC_000017.10:g.7979640C>T , CM000679.1:g.7979640C>T | GRCh37 |
| NC_000017.9:g.7920365C>T | NCBI36 |
| NG_007099.1:g.16382G>A | |
| NG_007099.2:g.16395G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001139.3:c.1385G>A MANE Select | NP_001130.1:p.Gly462Asp |
| ENST00000647874.1:c.1385G>A MANE Select | ENSP00000497784.1:p.Gly462Asp |
| NM_001139.2:c.1385G>A | NP_001130.1:p.Gly462Asp |
| ENST00000319144.4:c.1385G>A | ENSP00000315167.4:p.Gly462Asp |
| ENST00000577351.5:n.332G>A | |
| ENST00000583276.5:n.769G>A | |
| ENST00000584116.1:n.641G>A | |
| ENST00000649809.1:c.449G>A | ENSP00000496845.1:p.Gly150Asp |