Canonical Allele Identifier: CA2739279434
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2863026
ClinVar RCV Id: RCV003700112
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660791dup , CM000669.2:g.152660791dup GRCh38
NC_000007.13:g.152357876dup , CM000669.1:g.152357876dup GRCh37
NC_000007.12:g.151988809dup NCBI36
NG_027988.1:g.20378dup
NG_027988.2:g.20378dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11425dup ENSP00000513758.1:n.-47-11425dup
ENST00000698507.1:n.108-6dup
ENST00000359321.2:c.40-6dup MANE Select ENSP00000352271.1:n.40-6dup
ENST00000359321.1:c.40-6dup ENSP00000352271.1:n.40-6dup
ENST00000495707.1:n.62-6dup
NM_005431.1:c.40-6dup NP_005422.1:n.40-6dup
NM_005431.2:c.40-6dup MANE Select NP_005422.1:n.40-6dup
Search 100 bp 5'
Search 100 bp 3'