Canonical Allele Identifier: CA762418636

Gene: STAT4

Linked Data

• dbSNP Id: rs1008623175
• gnomAD v3: 2-191057091-G-A
• gnomAD v4: 2-191057091-G-A
• MyVariant Identifiers: chr2:g.191921817G>A (hg19) ; chr2:g.191057091G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191057091G>A , CM000664.2:g.191057091G>A	GRCh38
NC_000002.11:g.191921817G>A , CM000664.1:g.191921817G>A	GRCh37
NC_000002.10:g.191630062G>A	NCBI36
NG_012852.1:g.99109C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392320.7:c.1206+927C>T MANE Select	ENSP00000376134.2:n.1206+927C>T
ENST00000358470.8:c.1206+927C>T	ENSP00000351255.4:n.1206+927C>T
ENST00000392320.6:c.1206+927C>T	ENSP00000376134.2:n.1206+927C>T
ENST00000495849.5:n.1274+927C>T
NM_001243835.1:c.1206+927C>T	NP_001230764.1:n.1206+927C>T
NM_003151.3:c.1206+927C>T	NP_003142.1:n.1206+927C>T
XM_005246817.3:c.1233+927C>T	XP_005246874.1:n.1233+927C>T
XM_006712719.2:c.1206+927C>T	XP_006712782.1:n.1206+927C>T
XM_011511704.1:c.1233+927C>T	XP_011510006.1:n.1233+927C>T
XM_011511705.1:c.1206+927C>T	XP_011510007.1:n.1206+927C>T
XM_011511706.1:c.1233+927C>T	XP_011510008.1:n.1233+927C>T
XM_006712719.3:c.1206+927C>T	XP_006712782.1:n.1206+927C>T
XM_011511705.2:c.1206+927C>T	XP_011510007.1:n.1206+927C>T
XM_017004784.2:c.1206+927C>T	XP_016860273.1:n.1206+927C>T
NM_003151.4:c.1206+927C>T MANE Select	NP_003142.1:n.1206+927C>T
NM_001243835.2:c.1206+927C>T	NP_001230764.1:n.1206+927C>T