Canonical Allele Identifier: CA753276395

Gene: XRCC6

Linked Data

• dbSNP Id: rs146105341
• gnomAD v3: 22-41621167-G-C
• gnomAD v4: 22-41621167-G-C
• MyVariant Identifiers: chr22:g.42017171G>C (hg19) ; chr22:g.41621167G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621167G>C , CM000684.2:g.41621167G>C	GRCh38
NC_000022.10:g.42017171G>C , CM000684.1:g.42017171G>C	GRCh37
NC_000022.9:g.40347117G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.7:c.-194G>C	ENSP00000353192.3:n.-194G>C
ENST00000428575.6:c.-231G>C	ENSP00000403679.3:n.-231G>C
NM_001288977.1:c.-194G>C	NP_001275906.1:n.-194G>C
NM_001288978.1:c.-231G>C	NP_001275907.1:n.-231G>C
NM_001469.4:c.-194G>C	NP_001460.1:n.-194G>C