Canonical Allele Identifier: CA1040535041
Gene: STAT4 HGNC NCBI

Linked Data

dbSNP Id: rs1698112235

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191100029T>C , CM000664.2:g.191100029T>C GRCh38
NC_000002.11:g.191964755T>C , CM000664.1:g.191964755T>C GRCh37
NC_000002.10:g.191673000T>C NCBI36
NG_012852.1:g.56171A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000392320.7:c.274-23704A>G MANE Select ENSP00000376134.2:n.274-23704A>G
ENST00000647167.1:c.274-23704A>G ENSP00000495153.1:n.274-23704A>G
ENST00000358470.8:c.274-23704A>G ENSP00000351255.4:n.274-23704A>G
ENST00000392320.6:c.274-23704A>G ENSP00000376134.2:n.274-23704A>G
ENST00000413064.5:c.193-23704A>G ENSP00000403238.1:n.193-23704A>G
ENST00000495326.1:n.344-23704A>G
ENST00000495849.5:n.342-23704A>G
NM_001243835.1:c.274-23704A>G NP_001230764.1:n.274-23704A>G
NM_003151.3:c.274-23704A>G NP_003142.1:n.274-23704A>G
XM_005246817.3:c.301-23704A>G XP_005246874.1:n.301-23704A>G
XM_006712719.2:c.274-23704A>G XP_006712782.1:n.274-23704A>G
XM_011511704.1:c.301-23704A>G XP_011510006.1:n.301-23704A>G
XM_011511705.1:c.274-23704A>G XP_011510007.1:n.274-23704A>G
XM_011511706.1:c.301-23704A>G XP_011510008.1:n.301-23704A>G
XM_006712719.3:c.274-23704A>G XP_006712782.1:n.274-23704A>G
XM_011511705.2:c.274-23704A>G XP_011510007.1:n.274-23704A>G
XM_017004784.2:c.274-23704A>G XP_016860273.1:n.274-23704A>G
NM_003151.4:c.274-23704A>G MANE Select NP_003142.1:n.274-23704A>G
NM_001243835.2:c.274-23704A>G NP_001230764.1:n.274-23704A>G