HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189035179C= , CM000664.2:g.189035179C= | GRCh38 |
NC_000002.11:g.189899905C= , CM000664.1:g.189899905C= | GRCh37 |
NC_000002.10:g.189608150C= | NCBI36 |
NG_011799.1:g.149701G= | |
NG_011799.2:g.149701G= | |
NG_011799.3:g.195123G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374866.9:c.4114-24G= MANE Select | ENSP00000364000.3:n.4114-24G= | |
ENST00000374866.7:c.4114-24G= | ENSP00000364000.3:n.4114-24G= | |
ENST00000618828.1:c.2953-24G= | ENSP00000482184.1:n.2953-24G= | |
NM_000393.3:c.4114-24G= | NP_000384.2:n.4114-24G= | |
XM_011510573.1:c.3976-24G= | XP_011508875.1:n.3976-24G= | |
NM_000393.4:c.4114-24G= | NP_000384.2:n.4114-24G= | |
XM_011510573.3:c.3976-24G= | XP_011508875.1:n.3976-24G= | |
NM_000393.5:c.4114-24G= MANE Select | NP_000384.2:n.4114-24G= |