Canonical Allele Identifier: CA693574764

Gene: SOCS2

Linked Data

• dbSNP Id: rs1168610829
• MyVariant Identifiers: chr12:g.93980070A>G (hg19) ; chr12:g.93586294A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586294A>G , CM000674.2:g.93586294A>G	GRCh38
NC_000012.11:g.93980070A>G , CM000674.1:g.93980070A>G	GRCh37
NC_000012.10:g.92504201A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11121A>G	XP_011537237.1:n.591+11121A>G