Canonical Allele Identifier: CA12601433
Gene: XRCC2 HGNC NCBI
COSMIC:
COSN514130 (not active)
COSN15663515 (not active)
MyVariant.info:
GRCh38 chr7:g.152676167C>G
GRCh37 chr7:g.152373252C>G
gnomAD v2:
7:152373252 C / G
gnomAD v3:
7:152676167 C / G
gnomAD v4:
chr7-152676167-C-G
Joint Max Group AF 0.23138064 (SAS)
Genomes Max Group AF 0.22308183 (NFE)
Exomes Max Group AF 0.23174528 (SAS)
ClinVar RCV:
RCV001677911
ClinVar Variation:
1265138
dbSNP:
3218384
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676167C>G , CM000669.2:g.152676167C>G GRCh38
NC_000007.13:g.152373252C>G , CM000669.1:g.152373252C>G GRCh37
NC_000007.12:g.152004185C>G NCBI36
NG_027988.1:g.4999G>C
NG_027988.2:g.4999G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-174G>C ENSP00000513758.1:n.-174G>C
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