Canonical Allele Identifier: CA242005043

Gene: SOCS2

Linked Data

• dbSNP Id: rs983463507
• gnomAD v3: 12-93586134-TAA-T
• gnomAD v4: 12-93586134-TAA-T
• MyVariant Identifiers: chr12:g.93979911_93979912del (hg19) ; chr12:g.93586135_93586136del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586136_93586137del , CM000674.2:g.93586136_93586137del	GRCh38
NC_000012.11:g.93979912_93979913del , CM000674.1:g.93979912_93979913del	GRCh37
NC_000012.10:g.92504043_92504044del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*377_*378del	XP_005269270.2:n.*377_*378del
XM_006719673.1:c.*377_*378del	XP_006719736.1:n.*377_*378del
XM_006719674.1:c.*377_*378del	XP_006719737.1:n.*377_*378del
XM_011538929.1:c.*377_*378del	XP_011537231.1:n.*377_*378del
XM_011538930.1:c.*377_*378del	XP_011537232.1:n.*377_*378del
XM_011538931.1:c.*377_*378del	XP_011537233.1:n.*377_*378del
XM_011538932.1:c.*377_*378del	XP_011537234.1:n.*377_*378del
XM_011538933.1:c.*377_*378del	XP_011537235.1:n.*377_*378del
XM_011538934.1:c.*377_*378del	XP_011537236.1:n.*377_*378del
XM_011538935.1:c.591+10963_591+10964del	XP_011537237.1:n.591+10963_591+10964del
XR_944810.1:n.1721_1722del