Canonical Allele Identifier: CA753276399
Gene: XRCC6 HGNC NCBI

Linked Data

dbSNP Id: rs1171386926
MyVariant Identifiers: chr22:g.42017173T>C (hg19) chr22:g.41621169T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621169T>C , CM000684.2:g.41621169T>C GRCh38
NC_000022.10:g.42017173T>C , CM000684.1:g.42017173T>C GRCh37
NC_000022.9:g.40347119T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360079.7:c.-192T>C ENSP00000353192.3:n.-192T>C
ENST00000428575.6:c.-229T>C ENSP00000403679.3:n.-229T>C
NM_001288977.1:c.-192T>C NP_001275906.1:n.-192T>C
NM_001288978.1:c.-229T>C NP_001275907.1:n.-229T>C
NM_001469.4:c.-192T>C NP_001460.1:n.-192T>C
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