Canonical Allele Identifier: CA324608708
Gene: XRCC6 HGNC NCBI

Linked Data

dbSNP Id: rs571540057
gnomAD v2: 22-42017230-A-T
gnomAD v3: 22-41621226-A-T
gnomAD v4: 22-41621226-A-T
MyVariant Identifiers: chr22:g.42017230A>T (hg19) chr22:g.41621226A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621226A>T , CM000684.2:g.41621226A>T GRCh38
NC_000022.10:g.42017230A>T , CM000684.1:g.42017230A>T GRCh37
NC_000022.9:g.40347176A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.7:c.-135A>T ENSP00000353192.3:n.-135A>T
ENST00000428575.6:c.-172A>T ENSP00000403679.3:n.-172A>T
NM_001288977.1:c.-135A>T NP_001275906.1:n.-135A>T
NM_001288978.1:c.-172A>T NP_001275907.1:n.-172A>T
NM_001469.4:c.-135A>T NP_001460.1:n.-135A>T
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