Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.74642427G>A , CM000671.2:g.74642427G>A | GRCh38 |
| NC_000009.11:g.77257343G>A , CM000671.1:g.77257343G>A | GRCh37 |
| NC_000009.10:g.76447163G>A | NCBI36 |
| NG_046926.2:g.150092G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_006914.4:c.249G>A MANE Select | NP_008845.2:p.Gly83= |
| ENST00000376896.8:c.249G>A MANE Select | ENSP00000366093.2:p.Gly83= |
| NM_001365023.1:c.282G>A | NP_001351952.1:p.Gly94= |
| NM_006914.3:c.249G>A | NP_008845.2:p.Gly83= |
| ENST00000376896.7:c.249G>A | ENSP00000366093.2:p.Gly83= |
| ENST00000396204.2:c.282G>A | ENSP00000379507.2:p.Gly94= |
| XR_929948.1:n.7C>T | |
| XR_929948.2:n.7C>T |