Canonical Allele Identifier: CA2055419818
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586414G= , CM000674.2:g.93586414G= GRCh38
NC_000012.11:g.93980190G= , CM000674.1:g.93980190G= GRCh37
NC_000012.10:g.92504321G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11241G= XP_011537237.1:n.591+11241G=