Canonical Allele Identifier: CA172069962

Gene: GATA4

Linked Data

• dbSNP Id: rs996057845
• MyVariant Identifiers: chr8:g.11560969C>G (hg19) ; chr8:g.11703460C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.11703460C>G , CM000670.2:g.11703460C>G	GRCh38
NC_000008.10:g.11560969C>G , CM000670.1:g.11560969C>G	GRCh37
NC_000008.9:g.11598378C>G	NCBI36
NG_008177.2:g.31542C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526974.1:c.-458+2682C>G	ENSP00000473598.1:n.-458+2682C>G
ENST00000528712.5:c.-6+2682C>G	ENSP00000435043.1:n.-6+2682C>G
ENST00000532977.1:c.-458+2682C>G	ENSP00000473671.1:n.-458+2682C>G
NM_001308094.1:c.-6+2682C>G	NP_001295023.1:n.-6+2682C>G
XM_005272386.1:c.-458+2682C>G	XP_005272443.1:n.-458+2682C>G
XM_006716248.1:c.-458+2682C>G	XP_006716311.1:n.-458+2682C>G
XM_011543817.1:c.-458+2682C>G	XP_011542119.1:n.-458+2682C>G
XM_011543818.1:c.-458+3003C>G	XP_011542120.1:n.-458+3003C>G
XM_011543817.3:c.-458+2682C>G	XP_011542119.1:n.-458+2682C>G
XM_011543818.2:c.-458+3003C>G	XP_011542120.1:n.-458+3003C>G
XM_017013312.2:c.-1302C>G	XP_016868801.1:n.-1302C>G
NM_001308094.2:c.-6+2682C>G	NP_001295023.1:n.-6+2682C>G