Canonical Allele Identifier: CA437796960
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214378C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487507C>T , CM000665.2:g.196487507C>T GRCh38
NC_000003.11:g.196214378C>T , CM000665.1:g.196214378C>T GRCh37
NC_000003.10:g.197698775C>T NCBI36
NG_023425.1:g.21262G>A , LRG_185:g.21262G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.450G>A MANE Select ENSP00000320898.3:p.Leu150=
ENST00000437070.1:c.*22G>A ENSP00000396712.1:n.*22G>A
NM_152617.3:c.450G>A , LRG_185t1:c.450G>A NP_689830.2:p.Leu150=
NM_152617.4:c.450G>A MANE Select NP_689830.2:p.Leu150=
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