Canonical Allele Identifier: CA437796727
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214339T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487468T>C , CM000665.2:g.196487468T>C GRCh38
NC_000003.11:g.196214339T>C , CM000665.1:g.196214339T>C GRCh37
NC_000003.10:g.197698736T>C NCBI36
NG_023425.1:g.21301A>G , LRG_185:g.21301A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.489A>G MANE Select ENSP00000320898.3:p.Lys163=
ENST00000437070.1:c.*61A>G ENSP00000396712.1:n.*61A>G
NM_152617.3:c.489A>G , LRG_185t1:c.489A>G NP_689830.2:p.Lys163=
NM_152617.4:c.489A>G MANE Select NP_689830.2:p.Lys163=
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