Canonical Allele Identifier: CA1007869375

Gene: GATAD2B

Linked Data

• dbSNP Id: rs1674594299
• gnomAD v3: 1-153819382-ACT-A
• gnomAD v4: 1-153819382-ACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819383_153819384del , CM000663.2:g.153819383_153819384del	GRCh38
NC_000001.10:g.153791859_153791860del , CM000663.1:g.153791859_153791860del	GRCh37
NC_000001.9:g.152058483_152058484del	NCBI36
NG_050988.1:g.108592_108593del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.42+222_42+223del	ENSP00000515408.1:n.42+222_42+223del
ENST00000368655.5:c.465+222_465+223del MANE Select	ENSP00000357644.4:n.465+222_465+223del
ENST00000368655.4:c.465+222_465+223del	ENSP00000357644.4:n.465+222_465+223del
ENST00000634401.1:c.465+222_465+223del	ENSP00000489313.1:n.465+222_465+223del
ENST00000634408.1:c.465+222_465+223del	ENSP00000489595.1:n.465+222_465+223del
ENST00000634544.1:c.465+222_465+223del	ENSP00000489184.1:n.465+222_465+223del
NM_020699.2:c.465+222_465+223del	NP_065750.1:n.465+222_465+223del
XM_005245364.3:c.465+222_465+223del	XP_005245421.1:n.465+222_465+223del
XM_006711469.2:c.465+222_465+223del	XP_006711532.1:n.465+222_465+223del
XM_011509808.1:c.465+222_465+223del	XP_011508110.1:n.465+222_465+223del
NM_020699.3:c.465+222_465+223del	NP_065750.1:n.465+222_465+223del
XM_005245364.4:c.465+222_465+223del	XP_005245421.1:n.465+222_465+223del
XM_024448621.1:c.465+222_465+223del	XP_024304389.1:n.465+222_465+223del
NM_020699.4:c.465+222_465+223del MANE Select	NP_065750.1:n.465+222_465+223del