Canonical Allele Identifier: CA762418654

Gene: STAT4

Linked Data

• dbSNP Id: rs1306591189
• MyVariant Identifiers: chr2:g.191921944C>T (hg19) ; chr2:g.191057218C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057218C>T , CM000664.2:g.191057218C>T	GRCh38
NC_000002.11:g.191921944C>T , CM000664.1:g.191921944C>T	GRCh37
NC_000002.10:g.191630189C>T	NCBI36
NG_012852.1:g.98982G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+800G>A MANE Select	ENSP00000376134.2:n.1206+800G>A
ENST00000358470.8:c.1206+800G>A	ENSP00000351255.4:n.1206+800G>A
ENST00000392320.6:c.1206+800G>A	ENSP00000376134.2:n.1206+800G>A
ENST00000495849.5:n.1274+800G>A
NM_001243835.1:c.1206+800G>A	NP_001230764.1:n.1206+800G>A
NM_003151.3:c.1206+800G>A	NP_003142.1:n.1206+800G>A
XM_005246817.3:c.1233+800G>A	XP_005246874.1:n.1233+800G>A
XM_006712719.2:c.1206+800G>A	XP_006712782.1:n.1206+800G>A
XM_011511704.1:c.1233+800G>A	XP_011510006.1:n.1233+800G>A
XM_011511705.1:c.1206+800G>A	XP_011510007.1:n.1206+800G>A
XM_011511706.1:c.1233+800G>A	XP_011510008.1:n.1233+800G>A
XM_006712719.3:c.1206+800G>A	XP_006712782.1:n.1206+800G>A
XM_011511705.2:c.1206+800G>A	XP_011510007.1:n.1206+800G>A
XM_017004784.2:c.1206+800G>A	XP_016860273.1:n.1206+800G>A
NM_003151.4:c.1206+800G>A MANE Select	NP_003142.1:n.1206+800G>A
NM_001243835.2:c.1206+800G>A	NP_001230764.1:n.1206+800G>A