Canonical Allele Identifier: CA1316350012
Gene: STAT4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.191153045T= , CM000664.2:g.191153045T= GRCh38
NC_000002.11:g.192017771T= , CM000664.1:g.192017771T= GRCh37
NC_000002.10:g.191726016T= NCBI36
NG_012852.1:g.3155A=

Transcript Alleles

HGVS Amino-acid Change
XM_005246817.3:c.27-4841A= XP_005246874.1:n.27-4841A=
XM_011511704.1:c.27-4841A= XP_011510006.1:n.27-4841A=
XM_011511705.1:c.-2+2173A= XP_011510007.1:n.-2+2173A=
XM_011511706.1:c.27-4841A= XP_011510008.1:n.27-4841A=
XM_011511705.2:c.-2+2173A= XP_011510007.1:n.-2+2173A=