Canonical Allele Identifier: CA693574612

Gene: SOCS2

Linked Data

• dbSNP Id: rs1483393581
• MyVariant Identifiers: chr12:g.93979666_93979671del (hg19) ; chr12:g.93585890_93585895del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93585892_93585897del , CM000674.2:g.93585892_93585897del	GRCh38
NC_000012.11:g.93979668_93979673del , CM000674.1:g.93979668_93979673del	GRCh37
NC_000012.10:g.92503799_92503804del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*133_*138del	XP_005269270.2:n.*133_*138del
XM_006719673.1:c.*133_*138del	XP_006719736.1:n.*133_*138del
XM_006719674.1:c.*133_*138del	XP_006719737.1:n.*133_*138del
XM_011538929.1:c.*133_*138del	XP_011537231.1:n.*133_*138del
XM_011538930.1:c.*133_*138del	XP_011537232.1:n.*133_*138del
XM_011538931.1:c.*133_*138del	XP_011537233.1:n.*133_*138del
XM_011538932.1:c.*133_*138del	XP_011537234.1:n.*133_*138del
XM_011538933.1:c.*133_*138del	XP_011537235.1:n.*133_*138del
XM_011538934.1:c.*133_*138del	XP_011537236.1:n.*133_*138del
XM_011538935.1:c.591+10719_591+10724del	XP_011537237.1:n.591+10719_591+10724del
XR_944810.1:n.1477_1482del