Canonical Allele Identifier: CA2055419855
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586475A= , CM000674.2:g.93586475A= GRCh38
NC_000012.11:g.93980251A= , CM000674.1:g.93980251A= GRCh37
NC_000012.10:g.92504382A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011538935.1:c.591+11302A= XP_011537237.1:n.591+11302A=