Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21011376T>C , CM000664.2:g.21011376T>C | GRCh38 |
| NC_000002.11:g.21234248T>C , CM000664.1:g.21234248T>C | GRCh37 |
| NC_000002.10:g.21087753T>C | NCBI36 |
| NG_011793.1:g.37698A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673739.2:c.*4798A>G | ENSP00000501110.2:n.*4798A>G | |
| ENST00000673739.1:c.5206A>G | ENSP00000501110.1:n.5206A>G | |
| ENST00000233242.5:c.5492A>G MANE Select | ENSP00000233242.1:p.Tyr1831Cys | |
| ENST00000616098.4:c.5492A>G | ENSP00000477990.1:p.Tyr1831Cys | |
| NM_000384.2:c.5492A>G | NP_000375.2:p.Tyr1831Cys | |
| XM_011532809.1:c.5492A>G | XP_011531111.1:p.Tyr1831Cys | |
| NM_000384.3:c.5492A>G MANE Select | NP_000375.3:p.Tyr1831Cys |