Canonical Allele Identifier: CA2055419851
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954585620

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586459G>A , CM000674.2:g.93586459G>A GRCh38
NC_000012.11:g.93980235G>A , CM000674.1:g.93980235G>A GRCh37
NC_000012.10:g.92504366G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11286G>A XP_011537237.1:n.591+11286G>A