Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.134498621A>G , CM000685.2:g.134498621A>G | GRCh38 |
| NC_000023.10:g.133632651A>G , CM000685.1:g.133632651A>G | GRCh37 |
| NC_000023.9:g.133460317A>G | NCBI36 |
| NG_012329.1:g.43477A>G | |
| NG_012329.2:g.43477A>G |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000194.3:c.546A>G MANE Select | NP_000185.1:p.Glu182= |
| ENST00000298556.8:c.546A>G MANE Select | ENSP00000298556.7:p.Glu182= |
| NM_000194.2:c.546A>G | NP_000185.1:p.Glu182= |
| ENST00000298556.7:c.546A>G | ENSP00000298556.7:p.Glu182= |
| ENST00000462974.5:n.704A>G | |
| ENST00000475720.1:n.504A>G | |
| XM_011531328.1:c.564A>G | XP_011529630.1:p.Glu188= |