Canonical Allele Identifier: CA2055419759
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586329A= , CM000674.2:g.93586329A= GRCh38
NC_000012.11:g.93980105A= , CM000674.1:g.93980105A= GRCh37
NC_000012.10:g.92504236A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11156A= XP_011537237.1:n.591+11156A=