Canonical Allele Identifier: CA2055419746
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs10492321

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11139T>C XP_011537237.1:n.591+11139T>C