Canonical Allele Identifier: CA437797915
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214432C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487561C>A , CM000665.2:g.196487561C>A GRCh38
NC_000003.11:g.196214432C>A , CM000665.1:g.196214432C>A GRCh37
NC_000003.10:g.197698829C>A NCBI36
NG_023425.1:g.21208G>T , LRG_185:g.21208G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.396G>T MANE Select ENSP00000320898.3:p.Arg132=
ENST00000437070.1:c.319G>T ENSP00000396712.1:p.Gly107Cys
NM_152617.3:c.396G>T , LRG_185t1:c.396G>T NP_689830.2:p.Arg132=
NM_152617.4:c.396G>T MANE Select NP_689830.2:p.Arg132=
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