LDH info

Canonical Allele Identifier: CA11134343
Gene: STAT4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10181656

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191105153G>C , CM000664.2:g.191105153G>C GRCh38
NC_000002.11:g.191969879G>C , CM000664.1:g.191969879G>C GRCh37
NC_000002.10:g.191678124G>C NCBI36
NG_012852.1:g.51047C>G

Transcript Alleles

HGVS Amino-acid change
NM_001243835.1:c.274-28828C>G VV NP_001230764.1:p.=
NM_003151.3:c.274-28828C>G VV NP_003142.1:p.=
XM_005246817.3:c.301-28828C>G XP_005246874.1:p.=
XM_006712719.2:c.274-28828C>G XP_006712782.1:p.=
XM_011511704.1:c.301-28828C>G XP_011510006.1:p.=
XM_011511705.1:c.274-28828C>G XP_011510007.1:p.=
XM_011511706.1:c.301-28828C>G XP_011510008.1:p.=
XM_006712719.3:c.274-28828C>G XP_006712782.1:p.=
XM_011511705.2:c.274-28828C>G XP_011510007.1:p.=
XM_017004784.2:c.274-28828C>G XP_016860273.1:p.=
NM_003151.4:c.274-28828C>G VV MANE Preferred NP_003142.1:p.=
ENST00000358470.8:c.274-28828C>G ENSP00000351255.4:p.=
ENST00000392320.6:c.274-28828C>G ENSP00000376134.2:p.=
ENST00000413064.5:c.193-28828C>G ENSP00000403238.1:p.=
ENST00000495326.1:n.344-28828C>G
ENST00000495849.5:n.342-28828C>G