Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.45824369C>A , CM000682.2:g.45824369C>A | GRCh38 |
| NC_000020.10:g.44453008C>A , CM000682.1:g.44453008C>A | GRCh37 |
| NC_000020.9:g.43886415C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_003279.3:c.237G>T MANE Select | NP_003270.1:p.Met79Ile |
| ENST00000372555.8:c.237G>T MANE Select | ENSP00000361636.3:p.Met79Ile |
| NM_003279.2:c.237G>T | NP_003270.1:p.Met79Ile |
| ENST00000372555.7:c.237G>T | ENSP00000361636.3:p.Met79Ile |
| ENST00000372557.1:c.192G>T | ENSP00000361638.1:p.Met64Ile |
| XM_011529031.1:c.192G>T | XP_011527333.1:p.Met64Ile |
| XM_011529031.2:c.192G>T | XP_011527333.1:p.Met64Ile |