Canonical Allele Identifier: CA242005077

Gene: SOCS2

Linked Data

• dbSNP Id: rs555655176
• gnomAD v3: 12-93586522-T-C
• gnomAD v4: 12-93586522-T-C
• MyVariant Identifiers: chr12:g.93980298T>C (hg19) ; chr12:g.93586522T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586522T>C , CM000674.2:g.93586522T>C	GRCh38
NC_000012.11:g.93980298T>C , CM000674.1:g.93980298T>C	GRCh37
NC_000012.10:g.92504429T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11349T>C	XP_011537237.1:n.591+11349T>C