Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429888T>C , CM000663.2:g.68429888T>C | GRCh38 |
| NC_000001.10:g.68895571T>C , CM000663.1:g.68895571T>C | GRCh37 |
| NC_000001.9:g.68668159T>C | NCBI36 |
| NG_008472.1:g.25072A>G | |
| NG_008472.2:g.25072A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1490A>G MANE Select | ENSP00000262340.5:p.Gln497Arg | |
| ENST00000262340.5:c.1490A>G | ENSP00000262340.5:p.Gln497Arg | |
| NM_000329.2:c.1490A>G | NP_000320.1:p.Gln497Arg | |
| XM_017002027.1:c.1214A>G | XP_016857516.1:p.Gln405Arg | |
| NM_000329.3:c.1490A>G MANE Select | NP_000320.1:p.Gln497Arg |