Canonical Allele Identifier: CA2055419741
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954584762

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586305T>C , CM000674.2:g.93586305T>C GRCh38
NC_000012.11:g.93980081T>C , CM000674.1:g.93980081T>C GRCh37
NC_000012.10:g.92504212T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11132T>C XP_011537237.1:n.591+11132T>C