Canonical Allele Identifier: CA355625344
Gene: RNF168 HGNC NCBI

Linked Data

COSMIC: COSM6330949
MyVariant Identifiers: chr3:g.196214359C>T (hg19) chr3:g.196487488C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487488C>T , CM000665.2:g.196487488C>T GRCh38
NC_000003.11:g.196214359C>T , CM000665.1:g.196214359C>T GRCh37
NC_000003.10:g.197698756C>T NCBI36
NG_023425.1:g.21281G>A , LRG_185:g.21281G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.469G>A MANE Select ENSP00000320898.3:p.Glu157Lys
ENST00000437070.1:c.*41G>A ENSP00000396712.1:n.*41G>A
NM_152617.3:c.469G>A , LRG_185t1:c.469G>A NP_689830.2:p.Glu157Lys
NM_152617.4:c.469G>A MANE Select NP_689830.2:p.Glu157Lys
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