Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755561C>T , CM000679.2:g.43755561C>T | GRCh38 |
| NC_000017.10:g.41832929C>T , CM000679.1:g.41832929C>T | GRCh37 |
| NC_000017.9:g.39188455C>T | NCBI36 |
| NG_008078.2:g.8228G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.423G>A MANE Select | ENSP00000301691.1:p.Ala141= | |
| ENST00000301691.2:c.423G>A | ENSP00000301691.1:p.Ala141= | |
| NM_025237.2:c.423G>A | NP_079513.1:p.Ala141= | |
| NM_025237.3:c.423G>A MANE Select | NP_079513.1:p.Ala141= |