Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.15443524C>T , CM000663.2:g.15443524C>T | GRCh38 |
| NC_000001.10:g.15770019C>T , CM000663.1:g.15770019C>T | GRCh37 |
| NC_000001.9:g.15642606C>T | NCBI36 |
| NG_009253.1:g.10082C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_007272.3:c.462C>T MANE Select | NP_009203.2:p.Pro154= |
| ENST00000375949.5:c.462C>T MANE Select | ENSP00000365116.4:p.Pro154= |
| NM_007272.2:c.462C>T | NP_009203.2:p.Pro154= |
| ENST00000375943.6:c.*62C>T | ENSP00000365110.2:n.*62C>T |
| ENST00000375949.4:c.462C>T | ENSP00000365116.4:p.Pro154= |
| ENST00000476813.5:n.284C>T | |
| ENST00000483406.1:n.372C>T | |
| XM_011540550.1:c.462C>T | XP_011538852.1:p.Pro154= |