Canonical Allele Identifier: CA693574814

Gene: SOCS2

Linked Data

• dbSNP Id: rs1472036551
• MyVariant Identifiers: chr12:g.93980278G>A (hg19) ; chr12:g.93586502G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586502G>A , CM000674.2:g.93586502G>A	GRCh38
NC_000012.11:g.93980278G>A , CM000674.1:g.93980278G>A	GRCh37
NC_000012.10:g.92504409G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11329G>A	XP_011537237.1:n.591+11329G>A