Canonical Allele Identifier: CA2055419377
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93585889_93585895delinsTATTTGC , CM000674.2:g.93585889_93585895delinsTATTTGC GRCh38
NC_000012.11:g.93979665_93979671delinsTATTTGC , CM000674.1:g.93979665_93979671delinsTATTTGC GRCh37
NC_000012.10:g.92503796_92503802delinsTATTTGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269213.3:c.*130_*136delinsTATTTGC XP_005269270.2:n.*130_*136delinsTATTTGC
XM_006719673.1:c.*130_*136delinsTATTTGC XP_006719736.1:n.*130_*136delinsTATTTGC
XM_006719674.1:c.*130_*136delinsTATTTGC XP_006719737.1:n.*130_*136delinsTATTTGC
XM_011538929.1:c.*130_*136delinsTATTTGC XP_011537231.1:n.*130_*136delinsTATTTGC
XM_011538930.1:c.*130_*136delinsTATTTGC XP_011537232.1:n.*130_*136delinsTATTTGC
XM_011538931.1:c.*130_*136delinsTATTTGC XP_011537233.1:n.*130_*136delinsTATTTGC
XM_011538932.1:c.*130_*136delinsTATTTGC XP_011537234.1:n.*130_*136delinsTATTTGC
XM_011538933.1:c.*130_*136delinsTATTTGC XP_011537235.1:n.*130_*136delinsTATTTGC
XM_011538934.1:c.*130_*136delinsTATTTGC XP_011537236.1:n.*130_*136delinsTATTTGC
XM_011538935.1:c.591+10716_591+10722delinsTATTTGC XP_011537237.1:n.591+10716_591+10722delinsTATTTGC
XR_944810.1:n.1474_1480delinsTATTTGC