Canonical Allele Identifier: CA2055419730
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586297G= , CM000674.2:g.93586297G= GRCh38
NC_000012.11:g.93980073G= , CM000674.1:g.93980073G= GRCh37
NC_000012.10:g.92504204G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11124G= XP_011537237.1:n.591+11124G=