Canonical Allele Identifier: CA355625246
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214338T>A (hg19) chr3:g.196487467T>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487467T>A , CM000665.2:g.196487467T>A GRCh38
NC_000003.11:g.196214338T>A , CM000665.1:g.196214338T>A GRCh37
NC_000003.10:g.197698735T>A NCBI36
NG_023425.1:g.21302A>T , LRG_185:g.21302A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.490A>T MANE Select ENSP00000320898.3:p.Arg164Trp
ENST00000437070.1:c.*62A>T ENSP00000396712.1:n.*62A>T
NM_152617.3:c.490A>T , LRG_185t1:c.490A>T NP_689830.2:p.Arg164Trp
NM_152617.4:c.490A>T MANE Select NP_689830.2:p.Arg164Trp
Search 100 bp 5'
Search 100 bp 3'