Canonical Allele Identifier: CA324608807

Gene: XRCC6

Linked Data

• dbSNP Id: rs1039922874
• gnomAD v3: 22-41621298-C-G
• gnomAD v4: 22-41621298-C-G
• MyVariant Identifiers: chr22:g.42017302C>G (hg19) ; chr22:g.41621298C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621298C>G , CM000684.2:g.41621298C>G	GRCh38
NC_000022.10:g.42017302C>G , CM000684.1:g.42017302C>G	GRCh37
NC_000022.9:g.40347248C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-63C>G MANE Select	ENSP00000353192.3:n.-63C>G
ENST00000360079.7:c.-63C>G	ENSP00000353192.3:n.-63C>G
ENST00000402580.7:c.-63C>G	ENSP00000384941.3:n.-63C>G
ENST00000428575.6:c.-100C>G	ENSP00000403679.3:n.-100C>G
ENST00000464116.2:n.14C>G
NM_001288977.1:c.-63C>G	NP_001275906.1:n.-63C>G
NM_001288978.1:c.-100C>G	NP_001275907.1:n.-100C>G
NM_001469.4:c.-63C>G	NP_001460.1:n.-63C>G
NM_001288976.2:c.-128C>G	NP_001275905.1:n.-128C>G
NM_001288977.2:c.-63C>G	NP_001275906.1:n.-63C>G
NM_001469.5:c.-63C>G MANE Select	NP_001460.1:n.-63C>G
NM_001288978.2:c.-100C>G	NP_001275907.1:n.-100C>G