Canonical Allele Identifier: CA1431675813
Gene: RNF168 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487466C= , CM000665.2:g.196487466C= GRCh38
NC_000003.11:g.196214337C= , CM000665.1:g.196214337C= GRCh37
NC_000003.10:g.197698734C= NCBI36
NG_023425.1:g.21303G= , LRG_185:g.21303G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.491G= MANE Select ENSP00000320898.3:p.Arg164=
ENST00000437070.1:c.*63G= ENSP00000396712.1:n.*63G=
NM_152617.3:c.491G= , LRG_185t1:c.491G= NP_689830.2:p.Arg164=
NM_152617.4:c.491G= MANE Select NP_689830.2:p.Arg164=
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