HGVS | Genome Assembly |
---|---|
NC_000014.9:g.77517921C= , CM000676.2:g.77517921C= | GRCh38 |
NC_000014.8:g.77984264C= , CM000676.1:g.77984264C= | GRCh37 |
NC_000014.7:g.77054017C= | NCBI36 |
NG_028282.1:g.103847G= , LRG_371:g.103847G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000686627.1:n.601+117G= | ||
ENST00000687688.1:n.1332+117G= | ||
ENST00000692906.1:n.1301+117G= | ||
ENST00000216484.7:c.1569+117G= MANE Select | ENSP00000216484.2:n.1569+117G= | |
ENST00000216484.6:c.1569+117G= | ENSP00000216484.2:n.1569+117G= | |
ENST00000556607.1:c.397+117G= | ENSP00000451029.1:n.397+117G= | |
NM_004863.3:c.1569+117G= , LRG_371t1:c.1569+117G= | NP_004854.1:n.1569+117G= | |
NM_004863.4:c.1569+117G= MANE Select | NP_004854.1:n.1569+117G= |