Canonical Allele Identifier: CA753276398

Gene: XRCC6

Linked Data

• dbSNP Id: rs1394151329
• gnomAD v3: 22-41621168-G-C
• gnomAD v4: 22-41621168-G-C
• MyVariant Identifiers: chr22:g.42017172G>C (hg19) ; chr22:g.41621168G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621168G>C , CM000684.2:g.41621168G>C	GRCh38
NC_000022.10:g.42017172G>C , CM000684.1:g.42017172G>C	GRCh37
NC_000022.9:g.40347118G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.7:c.-193G>C	ENSP00000353192.3:n.-193G>C
ENST00000428575.6:c.-230G>C	ENSP00000403679.3:n.-230G>C
NM_001288977.1:c.-193G>C	NP_001275906.1:n.-193G>C
NM_001288978.1:c.-230G>C	NP_001275907.1:n.-230G>C
NM_001469.4:c.-193G>C	NP_001460.1:n.-193G>C