Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.40793271G>A , CM000675.2:g.40793271G>A | GRCh38 |
| NC_000013.10:g.41367407G>A , CM000675.1:g.41367407G>A | GRCh37 |
| NC_000013.9:g.40265407G>A | NCBI36 |
| NG_012248.1:g.8861G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_014252.4:c.45G>A MANE Select | NP_055067.1:p.Ala15= |
| ENST00000338625.9:c.45G>A MANE Select | ENSP00000342267.4:p.Ala15= |
| NM_014252.3:c.45G>A | NP_055067.1:p.Ala15= |
| ENST00000338625.8:c.45G>A | ENSP00000342267.4:p.Ala15= |
| ENST00000417731.5:c.45G>A | ENSP00000415826.1:p.Ala15= |
| ENST00000470509.1:c.45G>A | ENSP00000431429.1:p.Ala15= |
| ENST00000478827.1:n.366G>A | |
| ENST00000707033.1:c.45G>A | ENSP00000516711.1:p.Ala15= |