Canonical Allele Identifier: CA2055419691
Gene: SOCS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586219A= , CM000674.2:g.93586219A= GRCh38
NC_000012.11:g.93979995A= , CM000674.1:g.93979995A= GRCh37
NC_000012.10:g.92504126A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XM_005269213.3:c.*460A= XP_005269270.2:n.*460A=
XM_006719673.1:c.*460A= XP_006719736.1:n.*460A=
XM_006719674.1:c.*460A= XP_006719737.1:n.*460A=
XM_011538929.1:c.*460A= XP_011537231.1:n.*460A=
XM_011538930.1:c.*460A= XP_011537232.1:n.*460A=
XM_011538931.1:c.*460A= XP_011537233.1:n.*460A=
XM_011538932.1:c.*460A= XP_011537234.1:n.*460A=
XM_011538933.1:c.*460A= XP_011537235.1:n.*460A=
XM_011538934.1:c.*460A= XP_011537236.1:n.*460A=
XM_011538935.1:c.591+11046A= XP_011537237.1:n.591+11046A=
XR_944810.1:n.1804A=