Canonical Allele Identifier: CA2055419659

Gene: SOCS2

Linked Data

• dbSNP Id: rs1954584135

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586186_93586188del , CM000674.2:g.93586186_93586188del	GRCh38
NC_000012.11:g.93979962_93979964del , CM000674.1:g.93979962_93979964del	GRCh37
NC_000012.10:g.92504093_92504095del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*427_*429del	XP_005269270.2:n.*427_*429del
XM_006719673.1:c.*427_*429del	XP_006719736.1:n.*427_*429del
XM_006719674.1:c.*427_*429del	XP_006719737.1:n.*427_*429del
XM_011538929.1:c.*427_*429del	XP_011537231.1:n.*427_*429del
XM_011538930.1:c.*427_*429del	XP_011537232.1:n.*427_*429del
XM_011538931.1:c.*427_*429del	XP_011537233.1:n.*427_*429del
XM_011538932.1:c.*427_*429del	XP_011537234.1:n.*427_*429del
XM_011538933.1:c.*427_*429del	XP_011537235.1:n.*427_*429del
XM_011538934.1:c.*427_*429del	XP_011537236.1:n.*427_*429del
XM_011538935.1:c.591+11013_591+11015del	XP_011537237.1:n.591+11013_591+11015del
XR_944810.1:n.1771_1773del