Canonical Allele Identifier: CA355625526
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214400T>C (hg19) chr3:g.196487529T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487529T>C , CM000665.2:g.196487529T>C GRCh38
NC_000003.11:g.196214400T>C , CM000665.1:g.196214400T>C GRCh37
NC_000003.10:g.197698797T>C NCBI36
NG_023425.1:g.21240A>G , LRG_185:g.21240A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.428A>G MANE Select ENSP00000320898.3:p.Glu143Gly
ENST00000437070.1:c.351A>G ENSP00000396712.1:p.Ter117Trp
NM_152617.3:c.428A>G , LRG_185t1:c.428A>G NP_689830.2:p.Glu143Gly
NM_152617.4:c.428A>G MANE Select NP_689830.2:p.Glu143Gly
Search 100 bp 5'
Search 100 bp 3'