Canonical Allele Identifier: CA1025888858

Gene: XRCC6

Linked Data

• dbSNP Id: rs2067600023
• gnomAD v3: 22-41621331-T-C
• gnomAD v4: 22-41621331-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.41621331T>C , CM000684.2:g.41621331T>C	GRCh38
NC_000022.10:g.42017335T>C , CM000684.1:g.42017335T>C	GRCh37
NC_000022.9:g.40347281T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360079.8:c.-30T>C MANE Select	ENSP00000353192.3:n.-30T>C
ENST00000360079.7:c.-30T>C	ENSP00000353192.3:n.-30T>C
ENST00000402580.7:c.-30T>C	ENSP00000384941.3:n.-30T>C
ENST00000428575.6:c.-67T>C	ENSP00000403679.3:n.-67T>C
ENST00000464116.2:n.47T>C
NM_001288977.1:c.-30T>C	NP_001275906.1:n.-30T>C
NM_001288978.1:c.-67T>C	NP_001275907.1:n.-67T>C
NM_001469.4:c.-30T>C	NP_001460.1:n.-30T>C
NM_001288976.2:c.-95T>C	NP_001275905.1:n.-95T>C
NM_001288977.2:c.-30T>C	NP_001275906.1:n.-30T>C
NM_001469.5:c.-30T>C MANE Select	NP_001460.1:n.-30T>C
NM_001288978.2:c.-67T>C	NP_001275907.1:n.-67T>C