Canonical Allele Identifier: CA693574761

Gene: SOCS2

Linked Data

• dbSNP Id: rs1366339218
• gnomAD v3: 12-93586257-T-C
• gnomAD v4: 12-93586257-T-C
• MyVariant Identifiers: chr12:g.93980033T>C (hg19) ; chr12:g.93586257T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586257T>C , CM000674.2:g.93586257T>C	GRCh38
NC_000012.11:g.93980033T>C , CM000674.1:g.93980033T>C	GRCh37
NC_000012.10:g.92504164T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*498T>C	XP_005269270.2:n.*498T>C
XM_006719673.1:c.*498T>C	XP_006719736.1:n.*498T>C
XM_006719674.1:c.*498T>C	XP_006719737.1:n.*498T>C
XM_011538929.1:c.*498T>C	XP_011537231.1:n.*498T>C
XM_011538930.1:c.*498T>C	XP_011537232.1:n.*498T>C
XM_011538931.1:c.*498T>C	XP_011537233.1:n.*498T>C
XM_011538932.1:c.*498T>C	XP_011537234.1:n.*498T>C
XM_011538933.1:c.*498T>C	XP_011537235.1:n.*498T>C
XM_011538934.1:c.*498T>C	XP_011537236.1:n.*498T>C
XM_011538935.1:c.591+11084T>C	XP_011537237.1:n.591+11084T>C
XR_944810.1:n.1842T>C