Canonical Allele Identifier: CA693574810
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1480756425
gnomAD v3: 12-93586483-CA-C
gnomAD v4: 12-93586483-CA-C
MyVariant Identifiers: chr12:g.93980260del (hg19) chr12:g.93586484del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586485del , CM000674.2:g.93586485del GRCh38
NC_000012.11:g.93980261del , CM000674.1:g.93980261del GRCh37
NC_000012.10:g.92504392del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11312del XP_011537237.1:n.591+11312del
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