Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270000C>T , CM000668.2:g.31270000C>T | GRCh38 |
| NC_000006.11:g.31237777C>T , CM000668.1:g.31237777C>T | GRCh37 |
| NC_000006.10:g.31345756C>T | NCBI36 |
| NG_029422.2:g.7132G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000376228.10:c.981G>A MANE Select | ENSP00000365402.5:p.Val327= | |
| ENST00000376228.9:c.981G>A | ENSP00000365402.5:p.Val327= | |
| ENST00000376237.8:c.*568G>A | ENSP00000365412.4:n.*568G>A | |
| ENST00000383329.7:c.981G>A | ENSP00000372819.3:p.Val327= | |
| ENST00000470363.5:n.299G>A | ||
| ENST00000487245.5:n.1340G>A | ||
| NM_002117.5:c.981G>A | NP_002108.4:p.Val327= | |
| NM_002117.6:c.981G>A MANE Select | NP_002108.4:p.Val327= |