Canonical Allele Identifier: CA538481530

Gene: STAT4

Linked Data

• dbSNP Id: rs1485726470
• gnomAD v2: 2-191902833-G-T
• gnomAD v3: 2-191038107-G-T
• gnomAD v4: 2-191038107-G-T
• MyVariant Identifiers: chr2:g.191902833G>T (hg19) ; chr2:g.191038107G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.191038107G>T , CM000664.2:g.191038107G>T	GRCh38
NC_000002.11:g.191902833G>T , CM000664.1:g.191902833G>T	GRCh37
NC_000002.10:g.191611078G>T	NCBI36
NG_012852.1:g.118093C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000392320.7:c.1434+1092C>A MANE Select	ENSP00000376134.2:n.1434+1092C>A
ENST00000358470.8:c.1434+1092C>A	ENSP00000351255.4:n.1434+1092C>A
ENST00000392320.6:c.1434+1092C>A	ENSP00000376134.2:n.1434+1092C>A
ENST00000470708.1:n.393+1092C>A
ENST00000495849.5:n.1502+1092C>A
NM_001243835.1:c.1434+1092C>A	NP_001230764.1:n.1434+1092C>A
NM_003151.3:c.1434+1092C>A	NP_003142.1:n.1434+1092C>A
XM_005246817.3:c.1461+1092C>A	XP_005246874.1:n.1461+1092C>A
XM_006712719.2:c.1434+1092C>A	XP_006712782.1:n.1434+1092C>A
XM_011511704.1:c.1461+1092C>A	XP_011510006.1:n.1461+1092C>A
XM_011511705.1:c.1434+1092C>A	XP_011510007.1:n.1434+1092C>A
XM_006712719.3:c.1434+1092C>A	XP_006712782.1:n.1434+1092C>A
XM_011511705.2:c.1434+1092C>A	XP_011510007.1:n.1434+1092C>A
NM_003151.4:c.1434+1092C>A MANE Select	NP_003142.1:n.1434+1092C>A
NM_001243835.2:c.1434+1092C>A	NP_001230764.1:n.1434+1092C>A