Canonical Allele Identifier: CA11205790

Gene: STAT4

Linked Data

• dbSNP Id: rs7561832
• gnomAD v2: 2-192010589-T-C
• gnomAD v3: 2-191145863-T-C
• gnomAD v4: 2-191145863-T-C
• MyVariant Identifiers: chr2:g.192010589T>C (hg19) ; chr2:g.191145863T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191145863T>C , CM000664.2:g.191145863T>C	GRCh38
NC_000002.11:g.192010589T>C , CM000664.1:g.192010589T>C	GRCh37
NC_000002.10:g.191718834T>C	NCBI36
NG_012852.1:g.10337A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.273+750A>G MANE Select	ENSP00000376134.2:n.273+750A>G
ENST00000647167.1:c.273+750A>G	ENSP00000495153.1:n.273+750A>G
ENST00000358470.8:c.273+750A>G	ENSP00000351255.4:n.273+750A>G
ENST00000392320.6:c.273+750A>G	ENSP00000376134.2:n.273+750A>G
ENST00000409995.5:c.273+750A>G	ENSP00000386288.1:n.273+750A>G
ENST00000413064.5:c.192+750A>G	ENSP00000403238.1:n.192+750A>G
ENST00000495326.1:n.343+750A>G
ENST00000495849.5:n.341+750A>G
NM_001243835.1:c.273+750A>G	NP_001230764.1:n.273+750A>G
NM_003151.3:c.273+750A>G	NP_003142.1:n.273+750A>G
XM_005246817.3:c.300+750A>G	XP_005246874.1:n.300+750A>G
XM_006712719.2:c.273+750A>G	XP_006712782.1:n.273+750A>G
XM_011511704.1:c.300+750A>G	XP_011510006.1:n.300+750A>G
XM_011511705.1:c.273+750A>G	XP_011510007.1:n.273+750A>G
XM_011511706.1:c.300+750A>G	XP_011510008.1:n.300+750A>G
XM_006712719.3:c.273+750A>G	XP_006712782.1:n.273+750A>G
XM_011511705.2:c.273+750A>G	XP_011510007.1:n.273+750A>G
XM_017004784.2:c.273+750A>G	XP_016860273.1:n.273+750A>G
NM_003151.4:c.273+750A>G MANE Select	NP_003142.1:n.273+750A>G
NM_001243835.2:c.273+750A>G	NP_001230764.1:n.273+750A>G