HGVS | Genome Assembly |
---|---|
NC_000011.10:g.128891380G= , CM000673.2:g.128891380G= | GRCh38 |
NC_000011.9:g.128761275G= , CM000673.1:g.128761275G= | GRCh37 |
NC_000011.8:g.128266485G= | NCBI36 |
NG_023406.2:g.4963G= , LRG_333:g.4963G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000529694.6:c.-352G= MANE Select | ENSP00000433295.1:n.-352G= | |
ENST00000529694.5:c.-352G= | ENSP00000433295.1:n.-352G= | |
NM_000890.4:c.-352G= | NP_000881.3:n.-352G= | |
NM_001354169.1:c.-441G= | NP_001341098.1:n.-441G= | |
NM_000890.5:c.-352G= MANE Select | NP_000881.3:n.-352G= | |
NM_001354169.2:c.-441G= | NP_001341098.1:n.-441G= |