Canonical Allele Identifier: CA355625235
Gene: RNF168 HGNC NCBI

Linked Data

ClinVar Variation Id: 2265091
ClinVar RCV Id: RCV002808598
MyVariant Identifiers: chr3:g.196214335G>C (hg19) chr3:g.196487464G>C (hg38)
JSON-LD

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.493C>G MANE Select ENSP00000320898.3:p.Arg165Gly
ENST00000437070.1:c.*65C>G ENSP00000396712.1:n.*65C>G
NM_152617.3:c.493C>G , LRG_185t1:c.493C>G NP_689830.2:p.Arg165Gly
NM_152617.4:c.493C>G MANE Select NP_689830.2:p.Arg165Gly
Search 100 bp 5'
Search 100 bp 3'