Canonical Allele Identifier: CA324608622

Gene: XRCC6

Linked Data

• dbSNP Id: rs910017059
• gnomAD v3: 22-41621182-G-A
• gnomAD v4: 22-41621182-G-A
• MyVariant Identifiers: chr22:g.42017186G>A (hg19) ; chr22:g.41621182G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621182G>A , CM000684.2:g.41621182G>A	GRCh38
NC_000022.10:g.42017186G>A , CM000684.1:g.42017186G>A	GRCh37
NC_000022.9:g.40347132G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.7:c.-179G>A	ENSP00000353192.3:n.-179G>A
ENST00000428575.6:c.-216G>A	ENSP00000403679.3:n.-216G>A
NM_001288977.1:c.-179G>A	NP_001275906.1:n.-179G>A
NM_001288978.1:c.-216G>A	NP_001275907.1:n.-216G>A
NM_001469.4:c.-179G>A	NP_001460.1:n.-179G>A