Canonical Allele Identifier: CA606966608

Gene: SOCS2

Linked Data

• dbSNP Id: rs1193078946
• gnomAD v2: 12-93980216-AT-A
• gnomAD v3: 12-93586440-AT-A
• gnomAD v4: 12-93586440-AT-A
• MyVariant Identifiers: chr12:g.93980217del (hg19) ; chr12:g.93586441del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.93586444del , CM000674.2:g.93586444del	GRCh38
NC_000012.11:g.93980220del , CM000674.1:g.93980220del	GRCh37
NC_000012.10:g.92504351del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XM_011538935.1:c.591+11271del	XP_011537237.1:n.591+11271del