Canonical Allele Identifier: CA324619918
Gene: XRCC6 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs132774

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41635949C>G , CM000684.2:g.41635949C>G GRCh38
NC_000022.9:g.40361899C>G NCBI36
NC_000022.10:g.42031953C>G , CM000684.1:g.42031953C>G GRCh37

Transcript Alleles

HGVS Amino-acid change
ENST00000359308.8:c.196-164C>G ENSP00000352257.4:p.=
ENST00000360079.7:c.196-164C>G ENSP00000353192.3:p.=
ENST00000402580.7:c.196-287C>G ENSP00000384941.3:p.=
ENST00000405506.2:c.46-164C>G ENSP00000384082.1:p.=
ENST00000405878.5:c.196-164C>G ENSP00000384257.1:p.=
ENST00000428575.6:c.46-164C>G ENSP00000403679.3:p.=
NM_001288976.1:c.196-164C>G NP_001275905.1:p.=
NM_001288977.1:c.196-287C>G NP_001275906.1:p.=
NM_001288978.1:c.46-164C>G NP_001275907.1:p.=
NM_001469.4:c.196-164C>G NP_001460.1:p.=