HGVS | Genome Assembly |
---|---|
NC_000004.12:g.68669895C>T , CM000666.2:g.68669895C>T | GRCh38 |
NC_000004.11:g.69535613C>T , CM000666.1:g.69535613C>T | GRCh37 |
NC_000004.10:g.69218208C>T | NCBI36 |
NG_052676.1:g.5882G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000338206.6:c.724G>A MANE Select | ENSP00000341045.5:p.Gly242Arg | |
ENST00000338206.5:c.724G>A | ENSP00000341045.5:p.Gly242Arg | |
ENST00000616841.4:c.724G>A | ENSP00000482004.1:p.Gly242Arg | |
NM_001076.3:c.724G>A | NP_001067.2:p.Gly242Arg | |
NM_001076.4:c.724G>A MANE Select | NP_001067.2:p.Gly242Arg |