Canonical Allele Identifier: CA2055419737
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1954584736

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586302_93586303insAA , CM000674.2:g.93586302_93586303insAA GRCh38
NC_000012.11:g.93980078_93980079insAA , CM000674.1:g.93980078_93980079insAA GRCh37
NC_000012.10:g.92504209_92504210insAA NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11129_591+11130insAA XP_011537237.1:n.591+11129_591+11130insAA