Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.176093060C>T , CM000664.2:g.176093060C>T | GRCh38 |
| NC_000002.11:g.176957788C>T , CM000664.1:g.176957788C>T | GRCh37 |
| NC_000002.10:g.176666034C>T | NCBI36 |
| NG_008137.1:g.5257C>T |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000523.4:c.170C>T MANE Select | NP_000514.2:p.Ala57Val |
| ENST00000392539.4:c.170C>T MANE Select | ENSP00000376322.3:p.Ala57Val |
| NM_000523.3:c.170C>T | NP_000514.2:p.Ala57Val |
| ENST00000392539.3:c.170C>T | ENSP00000376322.3:p.Ala57Val |
| XM_011511068.1:c.725-1420C>T | XP_011509370.1:n.725-1420C>T |
| XM_011511068.2:c.725-1420C>T | XP_011509370.1:n.725-1420C>T |