Canonical Allele Identifier: CA355625464
Gene: RNF168 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.196487516C>A , CM000665.2:g.196487516C>A GRCh38
NC_000003.11:g.196214387C>A , CM000665.1:g.196214387C>A GRCh37
NC_000003.10:g.197698784C>A NCBI36
NG_023425.1:g.21253G>T , LRG_185:g.21253G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000318037.3:c.441G>T MANE Select ENSP00000320898.3:p.Gln147His
ENST00000437070.1:c.*13G>T ENSP00000396712.1:n.*13G>T
NM_152617.3:c.441G>T , LRG_185t1:c.441G>T NP_689830.2:p.Gln147His
NM_152617.4:c.441G>T MANE Select NP_689830.2:p.Gln147His