HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891603C>A , CM000673.2:g.128891603C>A | GRCh38 |
NC_000011.9:g.128761498C>A , CM000673.1:g.128761498C>A | GRCh37 |
NC_000011.8:g.128266708C>A | NCBI36 |
NG_023406.2:g.5186C>A , LRG_333:g.5186C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-129C>A MANE Select | ENSP00000433295.1:n.-129C>A | |
ENST00000338350.4:c.-218C>A | ENSP00000339960.4:n.-218C>A | |
ENST00000529694.5:c.-129C>A | ENSP00000433295.1:n.-129C>A | |
NM_000890.3:c.-129C>A , LRG_333t1:c.-129C>A | NP_000881.3:n.-129C>A | |
NM_000890.4:c.-129C>A | NP_000881.3:n.-129C>A | |
NM_001354169.1:c.-218C>A | NP_001341098.1:n.-218C>A | |
NM_000890.5:c.-129C>A MANE Select | NP_000881.3:n.-129C>A | |
NM_001354169.2:c.-218C>A | NP_001341098.1:n.-218C>A |