Canonical Allele Identifier: CA950578937

Gene: SOCS2

Linked Data

• dbSNP Id: rs1954582131
• gnomAD v3: 12-93585911-A-C
• gnomAD v4: 12-93585911-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93585911A>C , CM000674.2:g.93585911A>C	GRCh38
NC_000012.11:g.93979687A>C , CM000674.1:g.93979687A>C	GRCh37
NC_000012.10:g.92503818A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_005269213.3:c.*152A>C	XP_005269270.2:n.*152A>C
XM_006719673.1:c.*152A>C	XP_006719736.1:n.*152A>C
XM_006719674.1:c.*152A>C	XP_006719737.1:n.*152A>C
XM_011538929.1:c.*152A>C	XP_011537231.1:n.*152A>C
XM_011538930.1:c.*152A>C	XP_011537232.1:n.*152A>C
XM_011538931.1:c.*152A>C	XP_011537233.1:n.*152A>C
XM_011538932.1:c.*152A>C	XP_011537234.1:n.*152A>C
XM_011538933.1:c.*152A>C	XP_011537235.1:n.*152A>C
XM_011538934.1:c.*152A>C	XP_011537236.1:n.*152A>C
XM_011538935.1:c.591+10738A>C	XP_011537237.1:n.591+10738A>C
XR_944810.1:n.1496A>C