Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.212883378G>A , CM000663.2:g.212883378G>A | GRCh38 |
| NC_000001.10:g.213056720G>A , CM000663.1:g.213056720G>A | GRCh37 |
| NC_000001.9:g.211123343G>A | NCBI36 |
| NG_028131.1:g.30124G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000366971.9:c.1032G>A MANE Select | ENSP00000355938.4:p.Met344Ile | |
| ENST00000366971.8:c.1032G>A | ENSP00000355938.4:p.Met344Ile | |
| ENST00000419102.1:c.428G>A | ||
| ENST00000474693.1:n.257G>A | ||
| NM_014053.3:c.1032G>A | NP_054772.1:p.Met344Ile | |
| XM_011509446.1:c.1032G>A | XP_011507748.1:p.Met344Ile | |
| XR_247024.1:n.1206G>A | ||
| XR_426771.1:n.1333G>A | ||
| XM_011509446.3:c.1032G>A | XP_011507748.1:p.Met344Ile | |
| XR_247024.3:n.1206G>A | ||
| NM_014053.4:c.1032G>A MANE Select | NP_054772.1:p.Met344Ile |