HGVS | Genome Assembly |
---|---|
NC_000011.10:g.89178613A= , CM000673.2:g.89178613A= | GRCh38 |
NC_000011.9:g.88911781A= , CM000673.1:g.88911781A= | GRCh37 |
NC_000011.8:g.88551429A= | NCBI36 |
NG_008748.1:g.5742A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000263321.6:c.660A= MANE Select | ENSP00000263321.4:p.Gln220= | |
ENST00000263321.5:c.660A= | ENSP00000263321.4:p.Gln220= | |
ENST00000526139.1:n.721A= | ||
NM_000372.4:c.660A= | NP_000363.1:p.Gln220= | |
XM_011542970.1:c.660A= | XP_011541272.1:p.Gln220= | |
XM_011542970.2:c.660A= | XP_011541272.1:p.Gln220= | |
XR_001748321.1:n.2718-65080T= | ||
XR_001748322.1:n.2733-65080T= | ||
NM_000372.5:c.660A= MANE Select | NP_000363.1:p.Gln220= |