Canonical Allele Identifier: CA242005070

Gene: SOCS2

Linked Data

• dbSNP Id: rs994122639
• gnomAD v3: 12-93586420-A-C
• gnomAD v4: 12-93586420-A-C
• MyVariant Identifiers: chr12:g.93980196A>C (hg19) ; chr12:g.93586420A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586420A>C , CM000674.2:g.93586420A>C	GRCh38
NC_000012.11:g.93980196A>C , CM000674.1:g.93980196A>C	GRCh37
NC_000012.10:g.92504327A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11247A>C	XP_011537237.1:n.591+11247A>C