Canonical Allele Identifier: CA169486909
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1181545
ClinVar RCV Id: RCV001538954
dbSNP Id: rs10707642
gnomAD v2: 7-152345498-GA-G
gnomAD v3: 7-152648413-GA-G
gnomAD v4: 7-152648413-GA-G
MyVariant Identifiers: chr7:g.152345502del (hg19) chr7:g.152345499del (hg19) chr7:g.152648417del (hg38) chr7:g.152648414del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648428del , CM000669.2:g.152648428del GRCh38
NC_000007.13:g.152345513del , CM000669.1:g.152345513del GRCh37
NC_000007.12:g.151976446del NCBI36
NG_027988.1:g.32752del
NG_027988.2:g.32752del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*228del ENSP00000513758.1:n.*228del
ENST00000359321.2:c.*228del MANE Select ENSP00000352271.1:n.*228del
ENST00000359321.1:c.*228del ENSP00000352271.1:n.*228del
ENST00000495707.1:n.1093del
NM_005431.1:c.*228del NP_005422.1:n.*228del
NM_005431.2:c.*228del MANE Select NP_005422.1:n.*228del
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