Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.186153840T>C , CM000663.2:g.186153840T>C | GRCh38 |
| NC_000001.10:g.186122972T>C , CM000663.1:g.186122972T>C | GRCh37 |
| NC_000001.9:g.184389595T>C | NCBI36 |
| NG_011841.1:g.424290T>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_031935.3:c.15109T>C MANE Select | NP_114141.2:p.Tyr5037His |
| ENST00000271588.9:c.15109T>C MANE Select | ENSP00000271588.4:p.Tyr5037His |
| NM_031935.2:c.15109T>C | NP_114141.2:p.Tyr5037His |
| ENST00000271588.8:c.15109T>C | ENSP00000271588.4:p.Tyr5037His |
| ENST00000475585.1:n.15T>C | |
| XM_011510037.1:c.14824T>C | XP_011508339.1:p.Tyr4942His |
| XM_011510038.1:c.15109T>C | XP_011508340.1:p.Tyr5037His |
| XM_011510038.3:c.15109T>C | XP_011508340.1:p.Tyr5037His |
| XM_017002437.1:c.13132T>C | XP_016857926.1:p.Tyr4378His |