Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.38691378A>G , CM000675.2:g.38691378A>G | GRCh38 |
| NC_000013.10:g.39265515A>G , CM000675.1:g.39265515A>G | GRCh37 |
| NC_000013.9:g.38163515A>G | NCBI36 |
| NG_008125.2:g.9343A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_207361.6:c.4034A>G MANE Select | NP_997244.4:p.Tyr1345Cys |
| ENST00000280481.9:c.4034A>G MANE Select | ENSP00000280481.7:p.Tyr1345Cys |
| NM_207361.5:c.4034A>G | NP_997244.4:p.Tyr1345Cys |
| ENST00000280481.8:c.4034A>G | ENSP00000280481.7:p.Tyr1345Cys |
| XM_011535057.1:c.4034A>G | XP_011533359.1:p.Tyr1345Cys |
| XM_017020554.1:c.4034A>G | XP_016876043.1:p.Tyr1345Cys |
| XR_941571.1:n.4342A>G | |
| XR_941571.2:n.4338A>G |