Canonical Allele Identifier: CA242005067

Gene: SOCS2

Linked Data

• dbSNP Id: rs766270407
• MyVariant Identifiers: chr12:g.93980119T>C (hg19) ; chr12:g.93586343T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586343T>C , CM000674.2:g.93586343T>C	GRCh38
NC_000012.11:g.93980119T>C , CM000674.1:g.93980119T>C	GRCh37
NC_000012.10:g.92504250T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11170T>C	XP_011537237.1:n.591+11170T>C