Canonical Allele Identifier: CA242005076
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs537430587
MyVariant Identifiers: chr12:g.93980254C>T (hg19) chr12:g.93586478C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586478C>T , CM000674.2:g.93586478C>T GRCh38
NC_000012.11:g.93980254C>T , CM000674.1:g.93980254C>T GRCh37
NC_000012.10:g.92504385C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11305C>T XP_011537237.1:n.591+11305C>T
Search 100 bp 5'
Search 100 bp 3'