Canonical Allele Identifier: CA919147417
Gene: SOCS2 HGNC NCBI

Linked Data

dbSNP Id: rs1592839015

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93585897del , CM000674.2:g.93585897del GRCh38
NC_000012.11:g.93979673del , CM000674.1:g.93979673del GRCh37
NC_000012.10:g.92503804del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269213.3:c.*138del XP_005269270.2:n.*138del
XM_006719673.1:c.*138del XP_006719736.1:n.*138del
XM_006719674.1:c.*138del XP_006719737.1:n.*138del
XM_011538929.1:c.*138del XP_011537231.1:n.*138del
XM_011538930.1:c.*138del XP_011537232.1:n.*138del
XM_011538931.1:c.*138del XP_011537233.1:n.*138del
XM_011538932.1:c.*138del XP_011537234.1:n.*138del
XM_011538933.1:c.*138del XP_011537235.1:n.*138del
XM_011538934.1:c.*138del XP_011537236.1:n.*138del
XM_011538935.1:c.591+10724del XP_011537237.1:n.591+10724del
XR_944810.1:n.1482del