Canonical Allele Identifier: CA1108867631
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2098040717
gnomAD v3: 7-152675737-A-AG
gnomAD v4: 7-152675737-A-AG
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675739dup , CM000669.2:g.152675739dup GRCh38
NC_000007.13:g.152372824dup , CM000669.1:g.152372824dup GRCh37
NC_000007.12:g.152003757dup NCBI36
NG_027988.1:g.5428dup
NG_027988.2:g.5428dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+303dup ENSP00000513758.1:n.-48+303dup
ENST00000698507.1:n.107+303dup
ENST00000359321.2:c.39+303dup MANE Select ENSP00000352271.1:n.39+303dup
ENST00000359321.1:c.39+303dup ENSP00000352271.1:n.39+303dup
NM_005431.1:c.39+303dup NP_005422.1:n.39+303dup
NM_005431.2:c.39+303dup MANE Select NP_005422.1:n.39+303dup
Search 100 bp 5'
Search 100 bp 3'