Canonical Allele Identifier: CA950579073

Gene: SOCS2

Linked Data

• dbSNP Id: rs1954584387
• gnomAD v3: 12-93586234-ATC-A
• gnomAD v4: 12-93586234-ATC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586236_93586237del , CM000674.2:g.93586236_93586237del	GRCh38
NC_000012.11:g.93980012_93980013del , CM000674.1:g.93980012_93980013del	GRCh37
NC_000012.10:g.92504143_92504144del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*477_*478del	XP_005269270.2:n.*477_*478del
XM_006719673.1:c.*477_*478del	XP_006719736.1:n.*477_*478del
XM_006719674.1:c.*477_*478del	XP_006719737.1:n.*477_*478del
XM_011538929.1:c.*477_*478del	XP_011537231.1:n.*477_*478del
XM_011538930.1:c.*477_*478del	XP_011537232.1:n.*477_*478del
XM_011538931.1:c.*477_*478del	XP_011537233.1:n.*477_*478del
XM_011538932.1:c.*477_*478del	XP_011537234.1:n.*477_*478del
XM_011538933.1:c.*477_*478del	XP_011537235.1:n.*477_*478del
XM_011538934.1:c.*477_*478del	XP_011537236.1:n.*477_*478del
XM_011538935.1:c.591+11063_591+11064del	XP_011537237.1:n.591+11063_591+11064del
XR_944810.1:n.1821_1822del