Canonical Allele Identifier: CA2055419856
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1565846108

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586475A>G , CM000674.2:g.93586475A>G GRCh38
NC_000012.11:g.93980251A>G , CM000674.1:g.93980251A>G GRCh37
NC_000012.10:g.92504382A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11302A>G XP_011537237.1:n.591+11302A>G