Canonical Allele Identifier: CA2055419751
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954584895

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586319C>T , CM000674.2:g.93586319C>T GRCh38
NC_000012.11:g.93980095C>T , CM000674.1:g.93980095C>T GRCh37
NC_000012.10:g.92504226C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11146C>T XP_011537237.1:n.591+11146C>T