Linked Data
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80280304C>G , CM000672.2:g.80280304C>G | GRCh38 |
| NC_000010.10:g.82040060C>G , CM000672.1:g.82040060C>G | GRCh37 |
| NC_000010.9:g.82030040C>G | NCBI36 |
| NG_008083.1:g.14375G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.418G>C MANE Select | ENSP00000361287.3:p.Gly140Arg | |
| ENST00000372213.7:c.418G>C | ENSP00000361287.3:p.Gly140Arg | |
| ENST00000455001.1:c.229G>C | ENSP00000414961.1:p.Gly77Arg | |
| NM_000429.2:c.418G>C | NP_000420.1:p.Gly140Arg | |
| XM_005269842.3:c.418G>C | XP_005269899.1:p.Gly140Arg | |
| XM_005269843.3:c.295G>C | XP_005269900.1:p.Gly99Arg | |
| NM_000429.3:c.418G>C MANE Select | NP_000420.1:p.Gly140Arg |