Canonical Allele Identifier: CA14997468

Gene: XRCC6

Linked Data

• dbSNP Id: rs132770
• gnomAD v2: 22-42017264-A-G
• gnomAD v3: 22-41621260-A-G
• gnomAD v4: 22-41621260-A-G
• MyVariant Identifiers: chr22:g.42017264A>G (hg19) ; chr22:g.41621260A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621260A>G , CM000684.2:g.41621260A>G	GRCh38
NC_000022.10:g.42017264A>G , CM000684.1:g.42017264A>G	GRCh37
NC_000022.9:g.40347210A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000360079.7:c.-101A>G	ENSP00000353192.3:n.-101A>G
ENST00000428575.6:c.-138A>G	ENSP00000403679.3:n.-138A>G
NM_001288977.1:c.-101A>G	NP_001275906.1:n.-101A>G
NM_001288978.1:c.-138A>G	NP_001275907.1:n.-138A>G
NM_001469.4:c.-101A>G	NP_001460.1:n.-101A>G