Canonical Allele Identifier: CA950579148
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954585721

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586483C>A , CM000674.2:g.93586483C>A GRCh38
NC_000012.11:g.93980259C>A , CM000674.1:g.93980259C>A GRCh37
NC_000012.10:g.92504390C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11310C>A XP_011537237.1:n.591+11310C>A