Canonical Allele Identifier: CA242005064
Gene: SOCS2 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs10492321

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586312T>A , CM000674.2:g.93586312T>A GRCh38
NC_000012.11:g.93980088T>A , CM000674.1:g.93980088T>A GRCh37
NC_000012.10:g.92504219T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_011538935.1:c.591+11139T>A XP_011537237.1:p.=