Canonical Allele Identifier: CA355625260
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214341T>G (hg19) chr3:g.196487470T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487470T>G , CM000665.2:g.196487470T>G GRCh38
NC_000003.11:g.196214341T>G , CM000665.1:g.196214341T>G GRCh37
NC_000003.10:g.197698738T>G NCBI36
NG_023425.1:g.21299A>C , LRG_185:g.21299A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000318037.3:c.487A>C MANE Select ENSP00000320898.3:p.Lys163Gln
ENST00000437070.1:c.*59A>C ENSP00000396712.1:n.*59A>C
NM_152617.3:c.487A>C , LRG_185t1:c.487A>C NP_689830.2:p.Lys163Gln
NM_152617.4:c.487A>C MANE Select NP_689830.2:p.Lys163Gln
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