Canonical Allele Identifier: CA639458008
Gene: XRCC6 HGNC NCBI

Linked Data

dbSNP Id: rs1187962529
gnomAD v2: 22-42017167-G-A
gnomAD v3: 22-41621163-G-A
gnomAD v4: 22-41621163-G-A
MyVariant Identifiers: chr22:g.42017167G>A (hg19) chr22:g.41621163G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.41621163G>A , CM000684.2:g.41621163G>A GRCh38
NC_000022.10:g.42017167G>A , CM000684.1:g.42017167G>A GRCh37
NC_000022.9:g.40347113G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000360079.7:c.-198G>A ENSP00000353192.3:n.-198G>A
ENST00000428575.6:c.-235G>A ENSP00000403679.3:n.-235G>A
NM_001288977.1:c.-198G>A NP_001275906.1:n.-198G>A
NM_001288978.1:c.-235G>A NP_001275907.1:n.-235G>A
NM_001469.4:c.-198G>A NP_001460.1:n.-198G>A
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