Canonical Allele Identifier: CA606966602
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1355764130
gnomAD v2: 12-93980105-A-G
gnomAD v3: 12-93586329-A-G
gnomAD v4: 12-93586329-A-G
MyVariant Identifiers: chr12:g.93980105A>G (hg19) chr12:g.93586329A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586329A>G , CM000674.2:g.93586329A>G GRCh38
NC_000012.11:g.93980105A>G , CM000674.1:g.93980105A>G GRCh37
NC_000012.10:g.92504236A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11156A>G XP_011537237.1:n.591+11156A>G
Search 100 bp 5'
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