HGVS | Genome Assembly |
---|---|
NC_000023.11:g.153740343G>A , CM000685.2:g.153740343G>A | GRCh38 |
NC_000023.10:g.153005797G>A , CM000685.1:g.153005797G>A | GRCh37 |
NC_000023.9:g.152658991G>A | NCBI36 |
NG_009022.2:g.20476G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000218104.6:c.1634+106G>A MANE Select | ENSP00000218104.3:n.1634+106G>A | |
ENST00000218104.5:c.1634+106G>A | ENSP00000218104.3:n.1634+106G>A | |
ENST00000443684.2:n.637+106G>A | ||
NM_000033.3:c.1634+106G>A | NP_000024.2:n.1634+106G>A | |
XR_938507.1:n.2106+106G>A | ||
XR_938507.2:n.2106+106G>A | ||
NM_000033.4:c.1634+106G>A MANE Select | NP_000024.2:n.1634+106G>A |