Canonical Allele Identifier: CA437796707
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214335G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487464G>T , CM000665.2:g.196487464G>T GRCh38
NC_000003.11:g.196214335G>T , CM000665.1:g.196214335G>T GRCh37
NC_000003.10:g.197698732G>T NCBI36
NG_023425.1:g.21305C>A , LRG_185:g.21305C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.493C>A MANE Select ENSP00000320898.3:p.Arg165=
ENST00000437070.1:c.*65C>A ENSP00000396712.1:n.*65C>A
NM_152617.3:c.493C>A , LRG_185t1:c.493C>A NP_689830.2:p.Arg165=
NM_152617.4:c.493C>A MANE Select NP_689830.2:p.Arg165=
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Search 100 bp 3'