Canonical Allele Identifier: CA2619330592

Gene: STAT2

Linked Data

• gnomAD v4: 12-56342213-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56342213T>C , CM000674.2:g.56342213T>C	GRCh38
NC_000012.11:g.56735997T>C , CM000674.1:g.56735997T>C	GRCh37
NC_000012.10:g.55022264T>C	NCBI36
NG_046314.1:g.23041A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000555488.2:n.3615A>G
ENST00000698178.1:n.4323A>G
ENST00000698179.1:n.4275A>G
ENST00000698180.1:c.*3487A>G	ENSP00000513597.1:n.*3487A>G
ENST00000698181.1:n.4769A>G
ENST00000698182.1:n.4542A>G
ENST00000698183.1:n.5002A>G
ENST00000698184.1:n.4776A>G
ENST00000698185.1:n.4935A>G
ENST00000698186.1:c.*1176A>G	ENSP00000513598.1:n.*1176A>G
ENST00000698187.1:n.4047A>G
ENST00000698188.1:n.4399A>G
ENST00000698189.1:n.5809A>G
ENST00000698190.1:n.3956A>G
ENST00000698191.1:n.3889A>G
ENST00000698192.1:c.*742A>G	ENSP00000513599.1:n.*742A>G
ENST00000314128.9:c.*1176A>G MANE Select	ENSP00000315768.4:n.*1176A>G
ENST00000650805.1:c.*3166A>G	ENSP00000498710.1:n.*3166A>G
ENST00000651078.1:n.4385A>G
ENST00000651301.1:c.*3406A>G	ENSP00000498470.1:n.*3406A>G
ENST00000651805.1:n.4121A>G
ENST00000651915.1:c.*1176A>G	ENSP00000498876.1:n.*1176A>G
ENST00000651934.1:n.4172A>G
ENST00000652091.1:n.4250A>G
ENST00000652624.1:c.*2858A>G	ENSP00000499108.1:n.*2858A>G
ENST00000652741.1:c.*3487A>G	ENSP00000498704.1:n.*3487A>G
ENST00000556539.5:n.2662A>G
NM_005419.3:c.*1176A>G	NP_005410.1:n.*1176A>G
NM_198332.1:c.*1176A>G	NP_938146.1:n.*1176A>G
XM_011538697.2:c.*1176A>G	XP_011536999.1:n.*1176A>G
XM_011538698.3:c.*1176A>G	XP_011537000.1:n.*1176A>G
XM_011538700.2:c.*1176A>G	XP_011537002.1:n.*1176A>G
XM_017019904.2:c.*1176A>G	XP_016875393.1:n.*1176A>G
XR_001748856.1:n.3655A>G
XR_001748857.1:n.3736A>G
XR_001748858.2:n.3613A>G
XR_002957375.1:n.4027A>G
XR_002957376.1:n.3985A>G
NM_005419.4:c.*1176A>G MANE Select	NP_005410.1:n.*1176A>G
NM_198332.2:c.*1176A>G	NP_938146.1:n.*1176A>G
NM_001385110.1:c.*1176A>G	NP_001372039.1:n.*1176A>G
NM_001385111.1:c.*1176A>G	NP_001372040.1:n.*1176A>G
NM_001385113.1:c.*1301A>G	NP_001372042.1:n.*1301A>G
NM_001385114.1:c.*1176A>G	NP_001372043.1:n.*1176A>G
NM_001385115.1:c.*1176A>G	NP_001372044.1:n.*1176A>G