Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94015766G>T , CM000663.2:g.94015766G>T | GRCh38 |
| NC_000001.10:g.94481322G>T , CM000663.1:g.94481322G>T | GRCh37 |
| NC_000001.9:g.94253910G>T | NCBI36 |
| NG_009073.1:g.110384C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.5285C>A MANE Select | NP_000341.2:p.Ala1762Asp |
| ENST00000370225.4:c.5285C>A MANE Select | ENSP00000359245.3:p.Ala1762Asp |
| NM_000350.2:c.5285C>A | NP_000341.2:p.Ala1762Asp |
| ENST00000370225.3:c.5285C>A | ENSP00000359245.3:p.Ala1762Asp |
| ENST00000536513.5:c.1661C>A | ENSP00000439707.2:p.Ala554Asp |