Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.228165895C>A , CM000663.2:g.228165895C>A | GRCh38 |
| NC_000001.10:g.228353596C>A , CM000663.1:g.228353596C>A | GRCh37 |
| NC_000001.9:g.226420219C>A | NCBI36 |
| NG_042231.1:g.5088C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_001010867.4:c.79C>A MANE Select | NP_001010867.1:p.Pro27Thr |
| ENST00000366711.4:c.79C>A MANE Select | ENSP00000355672.3:p.Pro27Thr |
| NM_001010867.2:c.79C>A | NP_001010867.1:p.Pro27Thr |
| NM_001010867.3:c.79C>A | NP_001010867.1:p.Pro27Thr |
| ENST00000366711.3:c.79C>A | ENSP00000355672.3:p.Pro27Thr |
| XM_006711753.2:c.79C>A | XP_006711816.1:p.Pro27Thr |