Canonical Allele Identifier: CA242005046

Gene: SOCS2

Linked Data

• dbSNP Id: rs867491835
• gnomAD v2: 12-93979944-T-C
• gnomAD v3: 12-93586168-T-C
• gnomAD v4: 12-93586168-T-C
• MyVariant Identifiers: chr12:g.93979944T>C (hg19) ; chr12:g.93586168T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586168T>C , CM000674.2:g.93586168T>C	GRCh38
NC_000012.11:g.93979944T>C , CM000674.1:g.93979944T>C	GRCh37
NC_000012.10:g.92504075T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*409T>C	XP_005269270.2:n.*409T>C
XM_006719673.1:c.*409T>C	XP_006719736.1:n.*409T>C
XM_006719674.1:c.*409T>C	XP_006719737.1:n.*409T>C
XM_011538929.1:c.*409T>C	XP_011537231.1:n.*409T>C
XM_011538930.1:c.*409T>C	XP_011537232.1:n.*409T>C
XM_011538931.1:c.*409T>C	XP_011537233.1:n.*409T>C
XM_011538932.1:c.*409T>C	XP_011537234.1:n.*409T>C
XM_011538933.1:c.*409T>C	XP_011537235.1:n.*409T>C
XM_011538934.1:c.*409T>C	XP_011537236.1:n.*409T>C
XM_011538935.1:c.591+10995T>C	XP_011537237.1:n.591+10995T>C
XR_944810.1:n.1753T>C