Canonical Allele Identifier: CA693574768
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1490453871
MyVariant Identifiers: chr12:g.93980097A>G (hg19) chr12:g.93586321A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586321A>G , CM000674.2:g.93586321A>G GRCh38
NC_000012.11:g.93980097A>G , CM000674.1:g.93980097A>G GRCh37
NC_000012.10:g.92504228A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11148A>G XP_011537237.1:n.591+11148A>G
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