Canonical Allele Identifier: CA2055419727
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954584670

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586291C>T , CM000674.2:g.93586291C>T GRCh38
NC_000012.11:g.93980067C>T , CM000674.1:g.93980067C>T GRCh37
NC_000012.10:g.92504198C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11118C>T XP_011537237.1:n.591+11118C>T