Canonical Allele Identifier: CA606966609

Gene: SOCS2

Linked Data

• dbSNP Id: rs1442021456
• gnomAD v2: 12-93980265-G-T
• gnomAD v3: 12-93586489-G-T
• gnomAD v4: 12-93586489-G-T
• MyVariant Identifiers: chr12:g.93980265G>T (hg19) ; chr12:g.93586489G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586489G>T , CM000674.2:g.93586489G>T	GRCh38
NC_000012.11:g.93980265G>T , CM000674.1:g.93980265G>T	GRCh37
NC_000012.10:g.92504396G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11316G>T	XP_011537237.1:n.591+11316G>T