Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.4912591C>G , CM000674.2:g.4912591C>G | GRCh38 |
| NC_000012.11:g.5021757C>G , CM000674.1:g.5021757C>G | GRCh37 |
| NC_000012.10:g.4892018C>G | NCBI36 |
| NG_011815.1:g.7685C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000382545.5:c.1213C>G MANE Select | ENSP00000371985.3:p.Pro405Ala | |
| ENST00000543874.3:n.105+2119C>G | ||
| ENST00000639306.1:c.1051C>G | ENSP00000492506.1:p.Pro351Ala | |
| ENST00000639680.1:c.76+325C>G | ||
| ENST00000382545.3:c.1213C>G | ENSP00000371985.3:p.Pro405Ala | |
| ENST00000541095.1:n.105+2119C>G | ||
| ENST00000543874.2:n.96+2119C>G | ||
| NM_000217.2:c.1213C>G | NP_000208.2:p.Pro405Ala | |
| NM_000217.3:c.1213C>G MANE Select | NP_000208.2:p.Pro405Ala |