Canonical Allele Identifier: CA2055419776
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586345T= , CM000674.2:g.93586345T= GRCh38
NC_000012.11:g.93980121T= , CM000674.1:g.93980121T= GRCh37
NC_000012.10:g.92504252T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11172T= XP_011537237.1:n.591+11172T=