Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31269516C>G , CM000668.2:g.31269516C>G | GRCh38 |
| NC_000006.11:g.31237293C>G , CM000668.1:g.31237293C>G | GRCh37 |
| NC_000006.10:g.31345272C>G | NCBI36 |
| NG_029422.2:g.7616G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.1025G>C MANE Select | ENSP00000365402.5:p.Gly342Ala | |
| ENST00000376228.9:c.1025G>C | ENSP00000365402.5:p.Gly342Ala | |
| ENST00000376237.8:c.*612G>C | ENSP00000365412.4:n.*612G>C | |
| ENST00000383329.7:c.1043G>C | ENSP00000372819.3:p.Gly348Ala | |
| ENST00000466892.5:n.151G>C | ||
| ENST00000470363.5:n.783G>C | ||
| ENST00000487245.5:n.1384G>C | ||
| NM_002117.5:c.1025G>C | NP_002108.4:p.Gly342Ala | |
| NM_002117.6:c.1025G>C MANE Select | NP_002108.4:p.Gly342Ala |