Canonical Allele Identifier: CA2055419868
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954585766

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586492T>G , CM000674.2:g.93586492T>G GRCh38
NC_000012.11:g.93980268T>G , CM000674.1:g.93980268T>G GRCh37
NC_000012.10:g.92504399T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11319T>G XP_011537237.1:n.591+11319T>G