Canonical Allele Identifier: CA2619330562

Gene: STAT2

Linked Data

• gnomAD v4: 12-56342207-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56342207A>G , CM000674.2:g.56342207A>G	GRCh38
NC_000012.11:g.56735991A>G , CM000674.1:g.56735991A>G	GRCh37
NC_000012.10:g.55022258A>G	NCBI36
NG_046314.1:g.23047T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000555488.2:n.3621T>C
ENST00000698178.1:n.4329T>C
ENST00000698179.1:n.4281T>C
ENST00000698180.1:c.*3493T>C	ENSP00000513597.1:n.*3493T>C
ENST00000698181.1:n.4775T>C
ENST00000698182.1:n.4548T>C
ENST00000698183.1:n.5008T>C
ENST00000698184.1:n.4782T>C
ENST00000698185.1:n.4941T>C
ENST00000698186.1:c.*1182T>C	ENSP00000513598.1:n.*1182T>C
ENST00000698187.1:n.4053T>C
ENST00000698188.1:n.4405T>C
ENST00000698189.1:n.5815T>C
ENST00000698190.1:n.3962T>C
ENST00000698191.1:n.3895T>C
ENST00000698192.1:c.*748T>C	ENSP00000513599.1:n.*748T>C
ENST00000314128.9:c.*1182T>C MANE Select	ENSP00000315768.4:n.*1182T>C
ENST00000650805.1:c.*3172T>C	ENSP00000498710.1:n.*3172T>C
ENST00000651078.1:n.4391T>C
ENST00000651301.1:c.*3412T>C	ENSP00000498470.1:n.*3412T>C
ENST00000651805.1:n.4127T>C
ENST00000651915.1:c.*1182T>C	ENSP00000498876.1:n.*1182T>C
ENST00000651934.1:n.4178T>C
ENST00000652091.1:n.4256T>C
ENST00000652624.1:c.*2864T>C	ENSP00000499108.1:n.*2864T>C
ENST00000652741.1:c.*3493T>C	ENSP00000498704.1:n.*3493T>C
ENST00000556539.5:n.2668T>C
NM_005419.3:c.*1182T>C	NP_005410.1:n.*1182T>C
NM_198332.1:c.*1182T>C	NP_938146.1:n.*1182T>C
XM_011538697.2:c.*1182T>C	XP_011536999.1:n.*1182T>C
XM_011538698.3:c.*1182T>C	XP_011537000.1:n.*1182T>C
XM_011538700.2:c.*1182T>C	XP_011537002.1:n.*1182T>C
XM_017019904.2:c.*1182T>C	XP_016875393.1:n.*1182T>C
XR_001748856.1:n.3661T>C
XR_001748857.1:n.3742T>C
XR_001748858.2:n.3619T>C
XR_002957375.1:n.4033T>C
XR_002957376.1:n.3991T>C
NM_005419.4:c.*1182T>C MANE Select	NP_005410.1:n.*1182T>C
NM_198332.2:c.*1182T>C	NP_938146.1:n.*1182T>C
NM_001385110.1:c.*1182T>C	NP_001372039.1:n.*1182T>C
NM_001385111.1:c.*1182T>C	NP_001372040.1:n.*1182T>C
NM_001385113.1:c.*1307T>C	NP_001372042.1:n.*1307T>C
NM_001385114.1:c.*1182T>C	NP_001372043.1:n.*1182T>C
NM_001385115.1:c.*1182T>C	NP_001372044.1:n.*1182T>C