LDH info

Canonical Allele Identifier: CA172069820
Gene: GATA4 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 539983
ClinVar RCV Id: RCV000649894
dbSNP Id: rs769262495

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.11703355C>A , CM000670.2:g.11703355C>A GRCh38
NC_000008.10:g.11560864C>A , CM000670.1:g.11560864C>A GRCh37
NC_000008.9:g.11598273C>A NCBI36
NG_008177.2:g.31437C>A

Transcript Alleles

HGVS Amino-acid change
NM_001308094.1:c.-6+2577C>A VV NP_001295023.1:p.=
XM_005272386.1:c.-458+2577C>A XP_005272443.1:p.=
XM_006716248.1:c.-458+2577C>A XP_006716311.1:p.=
XM_011543817.1:c.-458+2577C>A XP_011542119.1:p.=
XM_011543818.1:c.-458+2898C>A XP_011542120.1:p.=
XM_011543817.3:c.-458+2577C>A XP_011542119.1:p.=
XM_011543818.2:c.-458+2898C>A XP_011542120.1:p.=
NM_001308094.2:c.-6+2577C>A VV NP_001295023.1:p.=
ENST00000526974.1:c.-458+2577C>A ENSP00000473598.1:p.=
ENST00000528712.5:c.-6+2577C>A ENSP00000435043.1:p.=
ENST00000532977.1:c.-458+2577C>A ENSP00000473671.1:p.=