Canonical Allele Identifier: CA342536007
Gene: GATAD2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819726C>G , CM000663.2:g.153819726C>G GRCh38
NC_000001.10:g.153792202C>G , CM000663.1:g.153792202C>G GRCh37
NC_000001.9:g.152058826C>G NCBI36
NG_050988.1:g.108250G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703630.1:c.-79G>C ENSP00000515408.1:n.-79G>C
ENST00000368655.5:c.345G>C MANE Select ENSP00000357644.4:p.Glu115Asp
ENST00000638051.1:n.63G>C
ENST00000368655.4:c.345G>C ENSP00000357644.4:p.Glu115Asp
ENST00000634401.1:c.345G>C ENSP00000489313.1:p.Glu115Asp
ENST00000634408.1:c.345G>C ENSP00000489595.1:p.Glu115Asp
ENST00000634544.1:c.345G>C ENSP00000489184.1:p.Glu115Asp
ENST00000634791.1:c.345G>C ENSP00000489566.1:p.Glu115Asp
NM_020699.2:c.345G>C NP_065750.1:p.Glu115Asp
XM_005245364.3:c.345G>C XP_005245421.1:p.Glu115Asp
XM_006711469.2:c.345G>C XP_006711532.1:p.Glu115Asp
XM_011509808.1:c.345G>C XP_011508110.1:p.Glu115Asp
NM_020699.3:c.345G>C NP_065750.1:p.Glu115Asp
XM_005245364.4:c.345G>C XP_005245421.1:p.Glu115Asp
XM_024448621.1:c.345G>C XP_024304389.1:p.Glu115Asp
NM_020699.4:c.345G>C MANE Select NP_065750.1:p.Glu115Asp