Canonical Allele Identifier: CA2055422783
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93589778C= , CM000674.2:g.93589778C= GRCh38
NC_000012.11:g.93983554C= , CM000674.1:g.93983554C= GRCh37
NC_000012.10:g.92507685C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+14605C= XP_011537237.1:n.591+14605C=