HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68670440G>T , CM000666.2:g.68670440G>T | GRCh38 |
NC_000004.11:g.69536158G>T , CM000666.1:g.69536158G>T | GRCh37 |
NC_000004.10:g.69218753G>T | NCBI36 |
NG_052676.1:g.5337C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.179C>A MANE Select | ENSP00000341045.5:p.Ala60Asp | |
ENST00000338206.5:c.179C>A | ENSP00000341045.5:p.Ala60Asp | |
ENST00000616841.4:c.179C>A | ENSP00000482004.1:p.Ala60Asp | |
NM_001076.3:c.179C>A | NP_001067.2:p.Ala60Asp | |
NM_001076.4:c.179C>A MANE Select | NP_001067.2:p.Ala60Asp |