Canonical Allele Identifier: CA2038329471
Gene: STAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1876688241

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56342208G>A , CM000674.2:g.56342208G>A GRCh38
NC_000012.11:g.56735992G>A , CM000674.1:g.56735992G>A GRCh37
NC_000012.10:g.55022259G>A NCBI36
NG_046314.1:g.23046C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000555488.2:n.3620C>T
ENST00000698178.1:n.4328C>T
ENST00000698179.1:n.4280C>T
ENST00000698180.1:c.*3492C>T ENSP00000513597.1:n.*3492C>T
ENST00000698181.1:n.4774C>T
ENST00000698182.1:n.4547C>T
ENST00000698183.1:n.5007C>T
ENST00000698184.1:n.4781C>T
ENST00000698185.1:n.4940C>T
ENST00000698186.1:c.*1181C>T ENSP00000513598.1:n.*1181C>T
ENST00000698187.1:n.4052C>T
ENST00000698188.1:n.4404C>T
ENST00000698189.1:n.5814C>T
ENST00000698190.1:n.3961C>T
ENST00000698191.1:n.3894C>T
ENST00000698192.1:c.*747C>T ENSP00000513599.1:n.*747C>T
ENST00000314128.9:c.*1181C>T MANE Select ENSP00000315768.4:n.*1181C>T
ENST00000650805.1:c.*3171C>T ENSP00000498710.1:n.*3171C>T
ENST00000651078.1:n.4390C>T
ENST00000651301.1:c.*3411C>T ENSP00000498470.1:n.*3411C>T
ENST00000651805.1:n.4126C>T
ENST00000651915.1:c.*1181C>T ENSP00000498876.1:n.*1181C>T
ENST00000651934.1:n.4177C>T
ENST00000652091.1:n.4255C>T
ENST00000652624.1:c.*2863C>T ENSP00000499108.1:n.*2863C>T
ENST00000652741.1:c.*3492C>T ENSP00000498704.1:n.*3492C>T
ENST00000556539.5:n.2667C>T
NM_005419.3:c.*1181C>T NP_005410.1:n.*1181C>T
NM_198332.1:c.*1181C>T NP_938146.1:n.*1181C>T
XM_011538697.2:c.*1181C>T XP_011536999.1:n.*1181C>T
XM_011538698.3:c.*1181C>T XP_011537000.1:n.*1181C>T
XM_011538700.2:c.*1181C>T XP_011537002.1:n.*1181C>T
XM_017019904.2:c.*1181C>T XP_016875393.1:n.*1181C>T
XR_001748856.1:n.3660C>T
XR_001748857.1:n.3741C>T
XR_001748858.2:n.3618C>T
XR_002957375.1:n.4032C>T
XR_002957376.1:n.3990C>T
NM_005419.4:c.*1181C>T MANE Select NP_005410.1:n.*1181C>T
NM_198332.2:c.*1181C>T NP_938146.1:n.*1181C>T
NM_001385110.1:c.*1181C>T NP_001372039.1:n.*1181C>T
NM_001385111.1:c.*1181C>T NP_001372040.1:n.*1181C>T
NM_001385113.1:c.*1306C>T NP_001372042.1:n.*1306C>T
NM_001385114.1:c.*1181C>T NP_001372043.1:n.*1181C>T
NM_001385115.1:c.*1181C>T NP_001372044.1:n.*1181C>T