Canonical Allele Identifier: CA355625511
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214397T>G (hg19) chr3:g.196487526T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487526T>G , CM000665.2:g.196487526T>G GRCh38
NC_000003.11:g.196214397T>G , CM000665.1:g.196214397T>G GRCh37
NC_000003.10:g.197698794T>G NCBI36
NG_023425.1:g.21243A>C , LRG_185:g.21243A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.431A>C MANE Select ENSP00000320898.3:p.Glu144Ala
ENST00000437070.1:c.*3A>C ENSP00000396712.1:n.*3A>C
NM_152617.3:c.431A>C , LRG_185t1:c.431A>C NP_689830.2:p.Glu144Ala
NM_152617.4:c.431A>C MANE Select NP_689830.2:p.Glu144Ala
Search 100 bp 5'
Search 100 bp 3'