LDH info

Canonical Allele Identifier: CA11093409
Gene: STAT4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs3821236

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191038032G>A , CM000664.2:g.191038032G>A GRCh38
NC_000002.11:g.191902758G>A , CM000664.1:g.191902758G>A GRCh37
NC_000002.10:g.191611003G>A NCBI36
NG_012852.1:g.118168C>T

Transcript Alleles

HGVS Amino-acid change
NM_001243835.1:c.1434+1167C>T VV NP_001230764.1:p.=
NM_003151.3:c.1434+1167C>T VV NP_003142.1:p.=
XM_005246817.3:c.1461+1167C>T XP_005246874.1:p.=
XM_006712719.2:c.1434+1167C>T XP_006712782.1:p.=
XM_011511704.1:c.1461+1167C>T XP_011510006.1:p.=
XM_011511705.1:c.1434+1167C>T XP_011510007.1:p.=
XM_006712719.3:c.1434+1167C>T XP_006712782.1:p.=
XM_011511705.2:c.1434+1167C>T XP_011510007.1:p.=
NM_003151.4:c.1434+1167C>T VV MANE Preferred NP_003142.1:p.=
NM_001243835.2:c.1434+1167C>T VV NP_001230764.1:p.=
ENST00000358470.8:c.1434+1167C>T ENSP00000351255.4:p.=
ENST00000392320.6:c.1434+1167C>T ENSP00000376134.2:p.=
ENST00000470708.1:n.393+1167C>T
ENST00000495849.5:n.1502+1167C>T