HGVS | Genome Assembly |
---|---|
NC_000001.11:g.183201883G= , CM000663.2:g.183201883G= | GRCh38 |
NC_000001.10:g.183171018G= , CM000663.1:g.183171018G= | GRCh37 |
NC_000001.9:g.181437641G= | NCBI36 |
NG_007079.2:g.20620G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264144.5:c.80-5998G= MANE Select | ENSP00000264144.4:n.80-5998G= | |
ENST00000264144.4:c.80-5998G= | ENSP00000264144.4:n.80-5998G= | |
ENST00000493293.5:c.80-5998G= | ENSP00000432063.1:n.80-5998G= | |
NM_005562.2:c.80-5998G= | NP_005553.2:n.80-5998G= | |
NM_018891.2:c.80-5998G= | NP_061486.2:n.80-5998G= | |
XM_017001273.2:c.80-5998G= | XP_016856762.1:n.80-5998G= | |
NM_005562.3:c.80-5998G= MANE Select | NP_005553.2:n.80-5998G= | |
NM_018891.3:c.80-5998G= | NP_061486.2:n.80-5998G= |