Canonical Allele Identifier: CA2038334609
Gene: STAT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56346816G= , CM000674.2:g.56346816G= GRCh38
NC_000012.11:g.56740600G= , CM000674.1:g.56740600G= GRCh37
NC_000012.10:g.55026867G= NCBI36
NG_046314.1:g.18438C=

Transcript Alleles

HGVS Amino-acid change
ENST00000555488.2:n.1260C=
ENST00000698178.1:n.2452+3C=
ENST00000698179.1:n.2404+3C=
ENST00000698180.1:c.*1616+3C= ENSP00000513597.1:n.*1616+3C=
ENST00000698181.1:n.2898+3C=
ENST00000698182.1:n.2671+3C=
ENST00000698183.1:n.3131+3C=
ENST00000698184.1:n.2714C=
ENST00000698185.1:n.3064+3C=
ENST00000698186.1:c.1729+3C= ENSP00000513598.1:n.1729+3C=
ENST00000698187.1:n.2187+3C=
ENST00000698188.1:n.2528+3C=
ENST00000698189.1:n.3645+3C=
ENST00000698190.1:n.2519+3C=
ENST00000698191.1:n.2452+3C=
ENST00000698192.1:c.1861+3C= ENSP00000513599.1:n.1861+3C=
ENST00000698193.1:c.1861+3C= ENSP00000513600.1:n.1861+3C=
ENST00000314128.9:c.1861+3C= MANE Select ENSP00000315768.4:n.1861+3C=
ENST00000556140.6:n.2633+3C=
ENST00000650805.1:c.*1295+3C= ENSP00000498710.1:n.*1295+3C=
ENST00000651078.1:n.2514+3C=
ENST00000651301.1:c.*1535+3C= ENSP00000498470.1:n.*1535+3C=
ENST00000651339.1:n.568+3C=
ENST00000651805.1:n.2250+3C=
ENST00000651915.1:c.1762+3C= ENSP00000498876.1:n.1762+3C=
ENST00000651934.1:n.2301+3C=
ENST00000651967.1:n.1976+3C=
ENST00000652091.1:n.2379+3C=
ENST00000652398.1:c.*1427+3C= ENSP00000499022.1:n.*1427+3C=
ENST00000652624.1:c.*987+3C= ENSP00000499108.1:n.*987+3C=
ENST00000652741.1:c.*1616+3C= ENSP00000498704.1:n.*1616+3C=
ENST00000314128.8:c.1861+3C= ENSP00000315768.4:n.1861+3C=
ENST00000555488.1:n.53C=
ENST00000556539.5:n.791+3C=
ENST00000557199.1:n.524C=
ENST00000557235.5:c.1849+3C= ENSP00000450751.1:n.1849+3C=
NM_005419.3:c.1861+3C= NP_005410.1:n.1861+3C=
NM_198332.1:c.1849+3C= NP_938146.1:n.1849+3C=
XM_011538697.1:c.1885+3C= XP_011536999.1:n.1885+3C=
XM_011538698.1:c.1873+3C= XP_011537000.1:n.1873+3C=
XM_011538700.1:c.1153+3C= XP_011537002.1:n.1153+3C=
XM_011538701.1:c.916+3C= XP_011537003.1:n.916+3C=
XM_011538697.2:c.1885+3C= XP_011536999.1:n.1885+3C=
XM_011538698.3:c.1873+3C= XP_011537000.1:n.1873+3C=
XM_011538700.2:c.1153+3C= XP_011537002.1:n.1153+3C=
XM_017019904.2:c.1129+3C= XP_016875393.1:n.1129+3C=
XR_001748856.1:n.1784+3C=
XR_001748857.1:n.1865+3C=
XR_001748858.2:n.1742+3C=
XR_002957375.1:n.2156+3C=
XR_002957376.1:n.2114+3C=
NM_005419.4:c.1861+3C= MANE Select NP_005410.1:n.1861+3C=
NM_198332.2:c.1849+3C= NP_938146.1:n.1849+3C=
NM_001385110.1:c.1828+3C= NP_001372039.1:n.1828+3C=
NM_001385111.1:c.1762+3C= NP_001372040.1:n.1762+3C=
NM_001385113.1:c.1861+3C= NP_001372042.1:n.1861+3C=
NM_001385114.1:c.1840+3C= NP_001372043.1:n.1840+3C=
NM_001385115.1:c.1819+3C= NP_001372044.1:n.1819+3C=