Canonical Allele Identifier: CA62701560
Gene: STAT4 HGNC NCBI

Linked Data

dbSNP Id: rs11889341

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191079016C>T , CM000664.2:g.191079016C>T GRCh38
NC_000002.11:g.191943742C>T , CM000664.1:g.191943742C>T GRCh37
NC_000002.10:g.191651987C>T NCBI36
NG_012852.1:g.77184G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392320.7:c.274-2691G>A MANE Select ENSP00000376134.2:n.274-2691G>A
ENST00000647167.1:c.274-2691G>A ENSP00000495153.1:n.274-2691G>A
ENST00000358470.8:c.274-2691G>A ENSP00000351255.4:n.274-2691G>A
ENST00000392320.6:c.274-2691G>A ENSP00000376134.2:n.274-2691G>A
ENST00000413064.5:c.193-2691G>A ENSP00000403238.1:n.193-2691G>A
ENST00000495326.1:n.344-2691G>A
ENST00000495849.5:n.342-2691G>A
NM_001243835.1:c.274-2691G>A NP_001230764.1:n.274-2691G>A
NM_003151.3:c.274-2691G>A NP_003142.1:n.274-2691G>A
XM_005246817.3:c.301-2691G>A XP_005246874.1:n.301-2691G>A
XM_006712719.2:c.274-2691G>A XP_006712782.1:n.274-2691G>A
XM_011511704.1:c.301-2691G>A XP_011510006.1:n.301-2691G>A
XM_011511705.1:c.274-2691G>A XP_011510007.1:n.274-2691G>A
XM_011511706.1:c.301-2691G>A XP_011510008.1:n.301-2691G>A
XM_006712719.3:c.274-2691G>A XP_006712782.1:n.274-2691G>A
XM_011511705.2:c.274-2691G>A XP_011510007.1:n.274-2691G>A
XM_017004784.2:c.274-2691G>A XP_016860273.1:n.274-2691G>A
NM_003151.4:c.274-2691G>A MANE Select NP_003142.1:n.274-2691G>A
NM_001243835.2:c.274-2691G>A NP_001230764.1:n.274-2691G>A