Canonical Allele Identifier: CA2648088549

Gene: GATAD2B

Linked Data

• gnomAD v4: 1-153812001-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.153812001A>T , CM000663.2:g.153812001A>T	GRCh38
NC_000001.10:g.153784477A>T , CM000663.1:g.153784477A>T	GRCh37
NC_000001.9:g.152051101A>T	NCBI36
NG_050988.1:g.115975T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000368655.5:c.1530+21T>A MANE Select	ENSP00000357644.4:n.1530+21T>A
ENST00000637918.1:c.17+21T>A
ENST00000368655.4:c.1530+21T>A	ENSP00000357644.4:n.1530+21T>A
ENST00000634408.1:c.1482+21T>A	ENSP00000489595.1:n.1482+21T>A
ENST00000634544.1:c.1530+21T>A	ENSP00000489184.1:n.1530+21T>A
ENST00000634564.1:c.784+21T>A
ENST00000634645.1:n.254+21T>A
NM_020699.2:c.1530+21T>A	NP_065750.1:n.1530+21T>A
XM_005245364.3:c.1530+21T>A	XP_005245421.1:n.1530+21T>A
XM_006711469.2:c.1530+21T>A	XP_006711532.1:n.1530+21T>A
XM_011509808.1:c.1530+21T>A	XP_011508110.1:n.1530+21T>A
NM_020699.3:c.1530+21T>A	NP_065750.1:n.1530+21T>A
XM_005245364.4:c.1530+21T>A	XP_005245421.1:n.1530+21T>A
XM_024448621.1:c.1530+21T>A	XP_024304389.1:n.1530+21T>A
NM_020699.4:c.1530+21T>A MANE Select	NP_065750.1:n.1530+21T>A