Canonical Allele Identifier: CA62687954

Gene: STAT4

Linked Data

• dbSNP Id: rs947796510
• MyVariant Identifiers: chr2:g.191921875A>C (hg19) ; chr2:g.191057149A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057149A>C , CM000664.2:g.191057149A>C	GRCh38
NC_000002.11:g.191921875A>C , CM000664.1:g.191921875A>C	GRCh37
NC_000002.10:g.191630120A>C	NCBI36
NG_012852.1:g.99051T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+869T>G MANE Select	ENSP00000376134.2:n.1206+869T>G
ENST00000358470.8:c.1206+869T>G	ENSP00000351255.4:n.1206+869T>G
ENST00000392320.6:c.1206+869T>G	ENSP00000376134.2:n.1206+869T>G
ENST00000495849.5:n.1274+869T>G
NM_001243835.1:c.1206+869T>G	NP_001230764.1:n.1206+869T>G
NM_003151.3:c.1206+869T>G	NP_003142.1:n.1206+869T>G
XM_005246817.3:c.1233+869T>G	XP_005246874.1:n.1233+869T>G
XM_006712719.2:c.1206+869T>G	XP_006712782.1:n.1206+869T>G
XM_011511704.1:c.1233+869T>G	XP_011510006.1:n.1233+869T>G
XM_011511705.1:c.1206+869T>G	XP_011510007.1:n.1206+869T>G
XM_011511706.1:c.1233+869T>G	XP_011510008.1:n.1233+869T>G
XM_006712719.3:c.1206+869T>G	XP_006712782.1:n.1206+869T>G
XM_011511705.2:c.1206+869T>G	XP_011510007.1:n.1206+869T>G
XM_017004784.2:c.1206+869T>G	XP_016860273.1:n.1206+869T>G
NM_003151.4:c.1206+869T>G MANE Select	NP_003142.1:n.1206+869T>G
NM_001243835.2:c.1206+869T>G	NP_001230764.1:n.1206+869T>G