Canonical Allele Identifier: CA753276518

Gene: XRCC6

Linked Data

• dbSNP Id: rs1392991480
• gnomAD v3: 22-41621323-T-C
• gnomAD v4: 22-41621323-T-C
• MyVariant Identifiers: chr22:g.42017327T>C (hg19) ; chr22:g.41621323T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621323T>C , CM000684.2:g.41621323T>C	GRCh38
NC_000022.10:g.42017327T>C , CM000684.1:g.42017327T>C	GRCh37
NC_000022.9:g.40347273T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-38T>C MANE Select	ENSP00000353192.3:n.-38T>C
ENST00000360079.7:c.-38T>C	ENSP00000353192.3:n.-38T>C
ENST00000402580.7:c.-38T>C	ENSP00000384941.3:n.-38T>C
ENST00000428575.6:c.-75T>C	ENSP00000403679.3:n.-75T>C
ENST00000464116.2:n.39T>C
NM_001288977.1:c.-38T>C	NP_001275906.1:n.-38T>C
NM_001288978.1:c.-75T>C	NP_001275907.1:n.-75T>C
NM_001469.4:c.-38T>C	NP_001460.1:n.-38T>C
NM_001288976.2:c.-103T>C	NP_001275905.1:n.-103T>C
NM_001288977.2:c.-38T>C	NP_001275906.1:n.-38T>C
NM_001469.5:c.-38T>C MANE Select	NP_001460.1:n.-38T>C
NM_001288978.2:c.-75T>C	NP_001275907.1:n.-75T>C