Canonical Allele Identifier: CA355625329
Gene: RNF168 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.196214356T>A (hg19) chr3:g.196487485T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487485T>A , CM000665.2:g.196487485T>A GRCh38
NC_000003.11:g.196214356T>A , CM000665.1:g.196214356T>A GRCh37
NC_000003.10:g.197698753T>A NCBI36
NG_023425.1:g.21284A>T , LRG_185:g.21284A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.472A>T MANE Select ENSP00000320898.3:p.Lys158Ter
ENST00000437070.1:c.*44A>T ENSP00000396712.1:n.*44A>T
NM_152617.3:c.472A>T , LRG_185t1:c.472A>T NP_689830.2:p.Lys158Ter
NM_152617.4:c.472A>T MANE Select NP_689830.2:p.Lys158Ter
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