Canonical Allele Identifier: CA1120854
Gene: GATAD2B HGNC NCBI

Linked Data

dbSNP Id: rs751274982
ExAC: 1:153792037 TAGAA / T
gnomAD v2: 1-153792037-TAGAA-T
gnomAD v3: 1-153819561-TAGAA-T
gnomAD v4: 1-153819561-TAGAA-T
MyVariant Identifiers: chr1:g.153792038_153792041del (hg19) chr1:g.153819562_153819565del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.153819562_153819565del , CM000663.2:g.153819562_153819565del GRCh38
NC_000001.10:g.153792038_153792041del , CM000663.1:g.153792038_153792041del GRCh37
NC_000001.9:g.152058662_152058665del NCBI36
NG_050988.1:g.108411_108414del

Transcript Alleles

HGVS Amino-acid change
ENST00000703630.1:c.42+41_42+44del ENSP00000515408.1:n.42+41_42+44del
ENST00000368655.5:c.465+41_465+44del MANE Select ENSP00000357644.4:n.465+41_465+44del
ENST00000368655.4:c.465+41_465+44del ENSP00000357644.4:n.465+41_465+44del
ENST00000634401.1:c.465+41_465+44del ENSP00000489313.1:n.465+41_465+44del
ENST00000634408.1:c.465+41_465+44del ENSP00000489595.1:n.465+41_465+44del
ENST00000634544.1:c.465+41_465+44del ENSP00000489184.1:n.465+41_465+44del
NM_020699.2:c.465+41_465+44del NP_065750.1:n.465+41_465+44del
XM_005245364.3:c.465+41_465+44del XP_005245421.1:n.465+41_465+44del
XM_006711469.2:c.465+41_465+44del XP_006711532.1:n.465+41_465+44del
XM_011509808.1:c.465+41_465+44del XP_011508110.1:n.465+41_465+44del
NM_020699.3:c.465+41_465+44del NP_065750.1:n.465+41_465+44del
XM_005245364.4:c.465+41_465+44del XP_005245421.1:n.465+41_465+44del
XM_024448621.1:c.465+41_465+44del XP_024304389.1:n.465+41_465+44del
NM_020699.4:c.465+41_465+44del MANE Select NP_065750.1:n.465+41_465+44del
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