Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.136046392A>G , CM000667.2:g.136046392A>G | GRCh38 |
| NC_000005.9:g.135382081A>G , CM000667.1:g.135382081A>G | GRCh37 |
| NC_000005.8:g.135409980A>G | NCBI36 |
| NG_012646.1:g.22498A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000442011.7:c.356A>G MANE Select | ENSP00000416330.2:p.Gln119Arg | |
| ENST00000442011.6:c.356A>G | ENSP00000416330.2:p.Gln119Arg | |
| ENST00000504185.5:n.513A>G | ||
| ENST00000506699.5:n.421A>G | ||
| ENST00000507018.5:c.273A>G | ||
| ENST00000515433.1:n.648A>G | ||
| NM_000358.2:c.356A>G | NP_000349.1:p.Gln119Arg | |
| NM_000358.3:c.356A>G MANE Select | NP_000349.1:p.Gln119Arg |