Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49633759C>T , CM000676.2:g.49633759C>T | GRCh38 |
| NC_000014.8:g.50100477C>T , CM000676.1:g.50100477C>T | GRCh37 |
| NC_000014.7:g.49170227C>T | NCBI36 |
| NG_013070.1:g.6472G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018139.3:c.1391G>A MANE Select | NP_060609.2:p.Gly464Asp |
| ENST00000298292.13:c.1391G>A MANE Select | ENSP00000298292.8:p.Gly464Asp |
| NM_001083908.1:c.1391G>A | NP_001077377.1:p.Gly464Asp |
| NM_001083908.2:c.1391G>A | NP_001077377.1:p.Gly464Asp |
| NM_001378453.1:c.-481G>A | NP_001365382.1:n.-481G>A |
| NM_018139.2:c.1391G>A | NP_060609.2:p.Gly464Asp |
| ENST00000298292.12:c.1391G>A | ENSP00000298292.8:p.Gly464Asp |
| ENST00000406043.3:c.1391G>A | ENSP00000384862.3:p.Gly464Asp |