HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670422G>T , CM000666.2:g.68670422G>T | GRCh38 |
NC_000004.11:g.69536140G>T , CM000666.1:g.69536140G>T | GRCh37 |
NC_000004.10:g.69218735G>T | NCBI36 |
NG_052676.1:g.5355C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.197C>A MANE Select | ENSP00000341045.5:p.Ala66Asp | |
ENST00000338206.5:c.197C>A | ENSP00000341045.5:p.Ala66Asp | |
ENST00000616841.4:c.197C>A | ENSP00000482004.1:p.Ala66Asp | |
NM_001076.3:c.197C>A | NP_001067.2:p.Ala66Asp | |
NM_001076.4:c.197C>A MANE Select | NP_001067.2:p.Ala66Asp |