Canonical Allele Identifier: CA2055419853
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586469T= , CM000674.2:g.93586469T= GRCh38
NC_000012.11:g.93980245T= , CM000674.1:g.93980245T= GRCh37
NC_000012.10:g.92504376T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11296T= XP_011537237.1:n.591+11296T=