Canonical Allele Identifier: CA242005072
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs558322441
gnomAD v2: 12-93980207-T-TA
gnomAD v3: 12-93586431-T-TA
gnomAD v4: 12-93586431-T-TA
MyVariant Identifiers: chr12:g.93980207_93980208insA (hg19) chr12:g.93586431_93586432insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586433dup , CM000674.2:g.93586433dup GRCh38
NC_000012.11:g.93980209dup , CM000674.1:g.93980209dup GRCh37
NC_000012.10:g.92504340dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11260dup XP_011537237.1:n.591+11260dup
Search 100 bp 5'
Search 100 bp 3'