Canonical Allele Identifier: CA15912304
Gene: STAT3 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1026916

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.42377817A>G , CM000679.2:g.42377817A>G GRCh38
NC_000017.10:g.40529835A>G , CM000679.1:g.40529835A>G GRCh37
NC_000017.9:g.37783361A>G NCBI36
NG_007370.1:g.15679T>C , LRG_112:g.15679T>C

Transcript Alleles

HGVS Amino-acid change
NM_003150.3:c.-2+10462T>C VV NP_003141.2:p.=
NM_139276.2:c.-24+10462T>C , LRG_112t1:c.-24+10462T>C NP_644805.1:p.=
NM_213662.1:c.-24+10462T>C VV NP_998827.1:p.=
XM_005257616.2:c.-5+10462T>C XP_005257673.2:p.=
XM_005257617.2:c.-2+10462T>C XP_005257674.2:p.=
XM_011525145.1:c.-5+10462T>C XP_011523447.1:p.=
XM_011525146.1:c.-5+10462T>C XP_011523448.1:p.=
XM_005257616.4:c.-5+10462T>C XP_005257673.2:p.=
XM_005257617.3:c.-2+10462T>C XP_005257674.2:p.=
XM_011525145.3:c.-5+10462T>C XP_011523447.1:p.=
XM_011525146.3:c.-5+10462T>C XP_011523448.1:p.=
XM_017024972.1:c.-2+10462T>C XP_016880461.1:p.=
XM_017024973.2:c.-5+10462T>C XP_016880462.1:p.=
XM_017024974.1:c.-2+10462T>C XP_016880463.1:p.=
XM_017024975.1:c.-24+10462T>C XP_016880464.1:p.=
XM_017024976.1:c.-24+10462T>C XP_016880465.1:p.=
XM_024450896.1:c.-24+10462T>C XP_024306664.1:p.=
ENST00000264657.9:c.-24+10462T>C ENSP00000264657.4:p.=
ENST00000389272.7:c.-167+10462T>C ENSP00000373923.3:p.=
ENST00000404395.3:c.-2+10462T>C ENSP00000384943.3:p.=
ENST00000585517.5:c.-5+10462T>C ENSP00000467000.1:p.=
ENST00000588065.1:c.-143-3611T>C ENSP00000467173.1:p.=
ENST00000588969.5:c.-2+10462T>C ENSP00000467985.1:p.=