Canonical Allele Identifier: CA1764051058
Gene: GATA4 HGNC NCBI

Linked Data

dbSNP Id: rs1799749332

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11703318G>C , CM000670.2:g.11703318G>C GRCh38
NC_000008.10:g.11560827G>C , CM000670.1:g.11560827G>C GRCh37
NC_000008.9:g.11598236G>C NCBI36
NG_008177.2:g.31400G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000526974.1:c.-458+2540G>C ENSP00000473598.1:n.-458+2540G>C
ENST00000528712.5:c.-6+2540G>C ENSP00000435043.1:n.-6+2540G>C
ENST00000532977.1:c.-458+2540G>C ENSP00000473671.1:n.-458+2540G>C
NM_001308094.1:c.-6+2540G>C NP_001295023.1:n.-6+2540G>C
XM_005272386.1:c.-458+2540G>C XP_005272443.1:n.-458+2540G>C
XM_006716248.1:c.-458+2540G>C XP_006716311.1:n.-458+2540G>C
XM_011543817.1:c.-458+2540G>C XP_011542119.1:n.-458+2540G>C
XM_011543818.1:c.-458+2861G>C XP_011542120.1:n.-458+2861G>C
XM_011543817.3:c.-458+2540G>C XP_011542119.1:n.-458+2540G>C
XM_011543818.2:c.-458+2861G>C XP_011542120.1:n.-458+2861G>C
NM_001308094.2:c.-6+2540G>C NP_001295023.1:n.-6+2540G>C