Canonical Allele Identifier: CA526369895

Gene: GATAD2B

Linked Data

• dbSNP Id: rs1466323931
• gnomAD v2: 1-153791762-CTTAGG-C
• gnomAD v3: 1-153819286-CTTAGG-C
• gnomAD v4: 1-153819286-CTTAGG-C
• MyVariant Identifiers: chr1:g.153791763_153791767del (hg19) ; chr1:g.153819287_153819291del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153819291_153819295del , CM000663.2:g.153819291_153819295del	GRCh38
NC_000001.10:g.153791767_153791771del , CM000663.1:g.153791767_153791771del	GRCh37
NC_000001.9:g.152058391_152058395del	NCBI36
NG_050988.1:g.108685_108689del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703630.1:c.42+315_42+319del	ENSP00000515408.1:n.42+315_42+319del
ENST00000368655.5:c.465+315_465+319del MANE Select	ENSP00000357644.4:n.465+315_465+319del
ENST00000368655.4:c.465+315_465+319del	ENSP00000357644.4:n.465+315_465+319del
ENST00000634401.1:c.465+315_465+319del	ENSP00000489313.1:n.465+315_465+319del
ENST00000634408.1:c.465+315_465+319del	ENSP00000489595.1:n.465+315_465+319del
ENST00000634544.1:c.465+315_465+319del	ENSP00000489184.1:n.465+315_465+319del
NM_020699.2:c.465+315_465+319del	NP_065750.1:n.465+315_465+319del
XM_005245364.3:c.465+315_465+319del	XP_005245421.1:n.465+315_465+319del
XM_006711469.2:c.465+315_465+319del	XP_006711532.1:n.465+315_465+319del
XM_011509808.1:c.465+315_465+319del	XP_011508110.1:n.465+315_465+319del
NM_020699.3:c.465+315_465+319del	NP_065750.1:n.465+315_465+319del
XM_005245364.4:c.465+315_465+319del	XP_005245421.1:n.465+315_465+319del
XM_024448621.1:c.465+315_465+319del	XP_024304389.1:n.465+315_465+319del
NM_020699.4:c.465+315_465+319del MANE Select	NP_065750.1:n.465+315_465+319del