Canonical Allele Identifier: CA8262460
Gene: GEMIN4 HGNC NCBI

Linked Data

dbSNP Id: rs775770182
gnomAD v2: 17-649083-C-G
gnomAD v4: 17-745843-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.745843C>G , CM000679.2:g.745843C>G GRCh38
NC_000017.10:g.649083C>G , CM000679.1:g.649083C>G GRCh37
NC_000017.9:g.595833C>G NCBI36
NG_046938.1:g.12030G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000319004.6:c.2200G>C MANE Select ENSP00000321706.5:p.Glu734Gln
ENST00000319004.5:c.2200G>C ENSP00000321706.5:p.Glu734Gln
ENST00000576778.1:c.2167G>C ENSP00000459565.1:p.Glu723Gln
NM_015721.2:c.2200G>C NP_056536.2:p.Glu734Gln
XM_005256667.3:c.2212G>C XP_005256724.1:p.Glu738Gln
XM_005256668.3:c.2212G>C XP_005256725.1:p.Glu738Gln
XM_005256670.3:c.2167G>C XP_005256727.1:p.Glu723Gln
XM_011523910.1:c.2212G>C XP_011522212.1:p.Glu738Gln
XM_011523911.1:c.2212G>C XP_011522213.1:p.Glu738Gln
XM_011523912.1:c.2167G>C XP_011522214.1:p.Glu723Gln
XM_011523913.1:c.2167G>C XP_011522215.1:p.Glu723Gln
XM_005256667.4:c.2212G>C XP_005256724.1:p.Glu738Gln
XM_005256670.5:c.2167G>C XP_005256727.1:p.Glu723Gln
XM_011523910.2:c.2212G>C XP_011522212.1:p.Glu738Gln
XM_011523911.2:c.2212G>C XP_011522213.1:p.Glu738Gln
XM_011523912.2:c.2167G>C XP_011522214.1:p.Glu723Gln
XM_011523913.2:c.2167G>C XP_011522215.1:p.Glu723Gln
XM_017024709.1:c.2212G>C XP_016880198.1:p.Glu738Gln
NM_015721.3:c.2200G>C MANE Select NP_056536.2:p.Glu734Gln