Canonical Allele Identifier: CA2055419409

Gene: SOCS2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93585935C= , CM000674.2:g.93585935C=	GRCh38
NC_000012.11:g.93979711C= , CM000674.1:g.93979711C=	GRCh37
NC_000012.10:g.92503842C=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*176C=	XP_005269270.2:n.*176C=
XM_006719673.1:c.*176C=	XP_006719736.1:n.*176C=
XM_006719674.1:c.*176C=	XP_006719737.1:n.*176C=
XM_011538929.1:c.*176C=	XP_011537231.1:n.*176C=
XM_011538930.1:c.*176C=	XP_011537232.1:n.*176C=
XM_011538931.1:c.*176C=	XP_011537233.1:n.*176C=
XM_011538932.1:c.*176C=	XP_011537234.1:n.*176C=
XM_011538933.1:c.*176C=	XP_011537235.1:n.*176C=
XM_011538934.1:c.*176C=	XP_011537236.1:n.*176C=
XM_011538935.1:c.591+10762C=	XP_011537237.1:n.591+10762C=
XR_944810.1:n.1520C=