Canonical Allele Identifier: CA324608606

Gene: XRCC6

Linked Data

• dbSNP Id: rs146105341
• gnomAD v2: 22-42017171-G-T
• gnomAD v3: 22-41621167-G-T
• gnomAD v4: 22-41621167-G-T
• MyVariant Identifiers: chr22:g.42017171G>T (hg19) ; chr22:g.41621167G>T (hg38)

Genomic Alleles

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

Transcript Alleles

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