HGVS | Genome Assembly |
---|---|
NC_000019.10:g.43552163G= , CM000681.2:g.43552163G= | GRCh38 |
NC_000019.9:g.44056315G= , CM000681.1:g.44056315G= | GRCh37 |
NC_000019.8:g.48748155G= | NCBI36 |
NG_033799.1:g.28416C= , LRG_784:g.28416C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000262887.10:c.936C= MANE Select | ENSP00000262887.5:p.Gly312= | |
ENST00000262887.9:c.936C= | ENSP00000262887.4:p.Gly312= | |
ENST00000543982.5:c.843C= | ENSP00000443671.1:p.Gly281= | |
ENST00000595789.5:n.1057C= | ||
ENST00000597811.5:c.546C= | ||
ENST00000598422.1:n.616C= | ||
NM_006297.2:c.936C= , LRG_784t1:c.936C= | NP_006288.2:p.Gly312= | |
NM_006297.3:c.936C= MANE Select | NP_006288.2:p.Gly312= |