Canonical Allele Identifier: CA342535853
Gene: GATAD2B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819713T>G , CM000663.2:g.153819713T>G GRCh38
NC_000001.10:g.153792189T>G , CM000663.1:g.153792189T>G GRCh37
NC_000001.9:g.152058813T>G NCBI36
NG_050988.1:g.108263A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000703630.1:c.-66A>C ENSP00000515408.1:n.-66A>C
ENST00000368655.5:c.358A>C MANE Select ENSP00000357644.4:p.Thr120Pro
ENST00000638051.1:n.76A>C
ENST00000368655.4:c.358A>C ENSP00000357644.4:p.Thr120Pro
ENST00000634401.1:c.358A>C ENSP00000489313.1:p.Thr120Pro
ENST00000634408.1:c.358A>C ENSP00000489595.1:p.Thr120Pro
ENST00000634544.1:c.358A>C ENSP00000489184.1:p.Thr120Pro
ENST00000634791.1:c.358A>C ENSP00000489566.1:p.Thr120Pro
NM_020699.2:c.358A>C NP_065750.1:p.Thr120Pro
XM_005245364.3:c.358A>C XP_005245421.1:p.Thr120Pro
XM_006711469.2:c.358A>C XP_006711532.1:p.Thr120Pro
XM_011509808.1:c.358A>C XP_011508110.1:p.Thr120Pro
NM_020699.3:c.358A>C NP_065750.1:p.Thr120Pro
XM_005245364.4:c.358A>C XP_005245421.1:p.Thr120Pro
XM_024448621.1:c.358A>C XP_024304389.1:p.Thr120Pro
NM_020699.4:c.358A>C MANE Select NP_065750.1:p.Thr120Pro