Canonical Allele Identifier: CA324619833

Gene: XRCC6

Linked Data

• dbSNP Id: rs1022287933
• gnomAD v3: 22-41635851-T-C
• gnomAD v4: 22-41635851-T-C
• MyVariant Identifiers: chr22:g.42031855T>C (hg19) ; chr22:g.41635851T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41635851T>C , CM000684.2:g.41635851T>C	GRCh38
NC_000022.10:g.42031855T>C , CM000684.1:g.42031855T>C	GRCh37
NC_000022.9:g.40361801T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.8:c.196-262T>C MANE Select	ENSP00000353192.3:n.196-262T>C
ENST00000359308.8:c.196-262T>C	ENSP00000352257.4:n.196-262T>C
ENST00000360079.7:c.196-262T>C	ENSP00000353192.3:n.196-262T>C
ENST00000402580.7:c.196-385T>C	ENSP00000384941.3:n.196-385T>C
ENST00000405506.2:c.46-262T>C	ENSP00000384082.1:n.46-262T>C
ENST00000405878.5:c.196-262T>C	ENSP00000384257.1:n.196-262T>C
ENST00000428575.6:c.46-262T>C	ENSP00000403679.3:n.46-262T>C
NM_001288976.1:c.196-262T>C	NP_001275905.1:n.196-262T>C
NM_001288977.1:c.196-385T>C	NP_001275906.1:n.196-385T>C
NM_001288978.1:c.46-262T>C	NP_001275907.1:n.46-262T>C
NM_001469.4:c.196-262T>C	NP_001460.1:n.196-262T>C
NM_001288976.2:c.196-262T>C	NP_001275905.1:n.196-262T>C
NM_001288977.2:c.196-385T>C	NP_001275906.1:n.196-385T>C
NM_001469.5:c.196-262T>C MANE Select	NP_001460.1:n.196-262T>C
NM_001288978.2:c.46-262T>C	NP_001275907.1:n.46-262T>C