Canonical Allele Identifier: CA2055419658
Gene: SOCS2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.93586181_93586184delinsGTTC , CM000674.2:g.93586181_93586184delinsGTTC GRCh38
NC_000012.11:g.93979957_93979960delinsGTTC , CM000674.1:g.93979957_93979960delinsGTTC GRCh37
NC_000012.10:g.92504088_92504091delinsGTTC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_005269213.3:c.*422_*425delinsGTTC XP_005269270.2:n.*422_*425delinsGTTC
XM_006719673.1:c.*422_*425delinsGTTC XP_006719736.1:n.*422_*425delinsGTTC
XM_006719674.1:c.*422_*425delinsGTTC XP_006719737.1:n.*422_*425delinsGTTC
XM_011538929.1:c.*422_*425delinsGTTC XP_011537231.1:n.*422_*425delinsGTTC
XM_011538930.1:c.*422_*425delinsGTTC XP_011537232.1:n.*422_*425delinsGTTC
XM_011538931.1:c.*422_*425delinsGTTC XP_011537233.1:n.*422_*425delinsGTTC
XM_011538932.1:c.*422_*425delinsGTTC XP_011537234.1:n.*422_*425delinsGTTC
XM_011538933.1:c.*422_*425delinsGTTC XP_011537235.1:n.*422_*425delinsGTTC
XM_011538934.1:c.*422_*425delinsGTTC XP_011537236.1:n.*422_*425delinsGTTC
XM_011538935.1:c.591+11008_591+11011delinsGTTC XP_011537237.1:n.591+11008_591+11011delinsGTTC
XR_944810.1:n.1766_1769delinsGTTC
Search 100 bp 5'
Search 100 bp 3'