Canonical Allele Identifier: CA172070007

Gene: GATA4

Linked Data

• dbSNP Id: rs904229513
• gnomAD v3: 8-11703528-A-T
• gnomAD v4: 8-11703528-A-T
• MyVariant Identifiers: chr8:g.11561037A>T (hg19) ; chr8:g.11703528A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11703528A>T , CM000670.2:g.11703528A>T	GRCh38
NC_000008.10:g.11561037A>T , CM000670.1:g.11561037A>T	GRCh37
NC_000008.9:g.11598446A>T	NCBI36
NG_008177.2:g.31610A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526974.1:c.-458+2750A>T	ENSP00000473598.1:n.-458+2750A>T
ENST00000528712.5:c.-6+2750A>T	ENSP00000435043.1:n.-6+2750A>T
ENST00000532977.1:c.-458+2750A>T	ENSP00000473671.1:n.-458+2750A>T
NM_001308094.1:c.-6+2750A>T	NP_001295023.1:n.-6+2750A>T
XM_005272386.1:c.-458+2750A>T	XP_005272443.1:n.-458+2750A>T
XM_006716248.1:c.-458+2750A>T	XP_006716311.1:n.-458+2750A>T
XM_011543817.1:c.-458+2750A>T	XP_011542119.1:n.-458+2750A>T
XM_011543818.1:c.-458+3071A>T	XP_011542120.1:n.-458+3071A>T
XM_011543817.3:c.-458+2750A>T	XP_011542119.1:n.-458+2750A>T
XM_011543818.2:c.-458+3071A>T	XP_011542120.1:n.-458+3071A>T
XM_017013312.2:c.-1234A>T	XP_016868801.1:n.-1234A>T
NM_001308094.2:c.-6+2750A>T	NP_001295023.1:n.-6+2750A>T