HGVS | Genome Assembly |
---|---|
NC_000011.10:g.118312717G>A , CM000673.2:g.118312717G>A | GRCh38 |
NC_000011.9:g.118183432G>A , CM000673.1:g.118183432G>A | GRCh37 |
NC_000011.8:g.117688642G>A | NCBI36 |
NG_007383.1:g.13138G>A , LRG_38:g.13138G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000361763.9:c.203G>A MANE Select | ENSP00000354566.4:p.Gly68Asp | |
ENST00000361763.8:c.203G>A | ENSP00000354566.4:p.Gly68Asp | |
ENST00000526146.5:n.749G>A | ||
ENST00000528435.5:n.756G>A | ||
ENST00000528600.1:c.185G>A | ENSP00000433975.1:p.Gly62Asp | |
ENST00000529713.5:n.309G>A | ||
ENST00000531913.1:n.574G>A | ||
NM_000733.3:c.203G>A , LRG_38t1:c.203G>A | NP_000724.1:p.Gly68Asp | |
NM_000733.4:c.203G>A MANE Select | NP_000724.1:p.Gly68Asp |