Canonical Allele Identifier: CA753276530

Gene: XRCC6

Linked Data

• dbSNP Id: rs1194099189
• gnomAD v3: 22-41621335-C-T
• gnomAD v4: 22-41621335-C-T
• MyVariant Identifiers: chr22:g.42017339C>T (hg19) ; chr22:g.41621335C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621335C>T , CM000684.2:g.41621335C>T	GRCh38
NC_000022.10:g.42017339C>T , CM000684.1:g.42017339C>T	GRCh37
NC_000022.9:g.40347285C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-26C>T MANE Select	ENSP00000353192.3:n.-26C>T
ENST00000360079.7:c.-26C>T	ENSP00000353192.3:n.-26C>T
ENST00000402580.7:c.-26C>T	ENSP00000384941.3:n.-26C>T
ENST00000428575.6:c.-63C>T	ENSP00000403679.3:n.-63C>T
ENST00000464116.2:n.51C>T
NM_001288977.1:c.-26C>T	NP_001275906.1:n.-26C>T
NM_001288978.1:c.-63C>T	NP_001275907.1:n.-63C>T
NM_001469.4:c.-26C>T	NP_001460.1:n.-26C>T
NM_001288976.2:c.-91C>T	NP_001275905.1:n.-91C>T
NM_001288977.2:c.-26C>T	NP_001275906.1:n.-26C>T
NM_001469.5:c.-26C>T MANE Select	NP_001460.1:n.-26C>T
NM_001288978.2:c.-63C>T	NP_001275907.1:n.-63C>T