Canonical Allele Identifier: CA693574813
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1179797865
MyVariant Identifiers: chr12:g.93980274C>A (hg19) chr12:g.93586498C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586498C>A , CM000674.2:g.93586498C>A GRCh38
NC_000012.11:g.93980274C>A , CM000674.1:g.93980274C>A GRCh37
NC_000012.10:g.92504405C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11325C>A XP_011537237.1:n.591+11325C>A
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