Canonical Allele Identifier: CA1025888751
Gene: XRCC6 HGNC NCBI

Linked Data

dbSNP Id: rs2067597038
gnomAD v3: 22-41621188-T-C
gnomAD v4: 22-41621188-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621188T>C , CM000684.2:g.41621188T>C GRCh38
NC_000022.10:g.42017192T>C , CM000684.1:g.42017192T>C GRCh37
NC_000022.9:g.40347138T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000360079.7:c.-173T>C ENSP00000353192.3:n.-173T>C
ENST00000428575.6:c.-210T>C ENSP00000403679.3:n.-210T>C
NM_001288977.1:c.-173T>C NP_001275906.1:n.-173T>C
NM_001288978.1:c.-210T>C NP_001275907.1:n.-210T>C
NM_001469.4:c.-173T>C NP_001460.1:n.-173T>C
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