Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.67259239C>A , CM000663.2:g.67259239C>A | GRCh38 |
| NC_000001.10:g.67724922C>A , CM000663.1:g.67724922C>A | GRCh37 |
| NC_000001.9:g.67497510C>A | NCBI36 |
| NG_011498.1:g.97754C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000347310.10:c.*111C>A MANE Select | ENSP00000321345.5:n.*111C>A | |
| ENST00000347310.9:c.*111C>A | ENSP00000321345.5:n.*111C>A | |
| ENST00000395227.2:c.*111C>A | ENSP00000378652.2:n.*111C>A | |
| ENST00000425614.3:c.*111C>A | ENSP00000387640.2:n.*111C>A | |
| ENST00000473881.2:c.*827C>A | ENSP00000486667.1:n.*827C>A | |
| NM_144701.2:c.*111C>A | NP_653302.2:n.*111C>A | |
| XM_005270516.2:c.*111C>A | XP_005270573.1:n.*111C>A | |
| XM_011540789.1:c.*111C>A | XP_011539091.1:n.*111C>A | |
| XM_011540790.1:c.*111C>A | XP_011539092.1:n.*111C>A | |
| XM_011540791.1:c.*111C>A | XP_011539093.1:n.*111C>A | |
| XM_011540790.3:c.*111C>A | XP_011539092.1:n.*111C>A | |
| XM_011540791.3:c.*111C>A | XP_011539093.1:n.*111C>A | |
| NM_144701.3:c.*111C>A MANE Select | NP_653302.2:n.*111C>A |