Canonical Allele Identifier: CA2055419735
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586302C= , CM000674.2:g.93586302C= GRCh38
NC_000012.11:g.93980078C= , CM000674.1:g.93980078C= GRCh37
NC_000012.10:g.92504209C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11129C= XP_011537237.1:n.591+11129C=