Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.56962023C>T , CM000678.2:g.56962023C>T | GRCh38 |
| NC_000016.9:g.56995935C>T , CM000678.1:g.56995935C>T | GRCh37 |
| NC_000016.8:g.55553436C>T | NCBI36 |
| NG_008952.1:g.5101C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000078.3:c.44C>T MANE Select | NP_000069.2:p.Ala15Val |
| ENST00000200676.8:c.44C>T MANE Select | ENSP00000200676.3:p.Ala15Val |
| NM_000078.2:c.44C>T | NP_000069.2:p.Ala15Val |
| NM_001286085.1:c.44C>T | NP_001273014.1:p.Ala15Val |
| NM_001286085.2:c.44C>T | NP_001273014.1:p.Ala15Val |
| ENST00000200676.7:c.44C>T | ENSP00000200676.3:p.Ala15Val |
| ENST00000379780.6:c.44C>T | ENSP00000369106.2:p.Ala15Val |
| ENST00000569082.1:n.42C>T | |
| XM_006721124.2:c.44C>T | XP_006721187.1:p.Ala15Val |
| XM_006721124.3:c.44C>T | XP_006721187.1:p.Ala15Val |