Canonical Allele Identifier: CA370199613
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2625103
ClinVar RCV Id: RCV003377782
dbSNP Id: rs1337184659
gnomAD v2: 7-152373146-T-C
MyVariant Identifiers: chr7:g.152373146T>C (hg19) chr7:g.152676061T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676061T>C , CM000669.2:g.152676061T>C GRCh38
NC_000007.13:g.152373146T>C , CM000669.1:g.152373146T>C GRCh37
NC_000007.12:g.152004079T>C NCBI36
NG_027988.1:g.5105A>G
NG_027988.2:g.5105A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-68A>G ENSP00000513758.1:n.-68A>G
ENST00000698507.1:n.87A>G
ENST00000359321.2:c.19A>G MANE Select ENSP00000352271.1:p.Arg7Gly
ENST00000359321.1:c.19A>G ENSP00000352271.1:p.Arg7Gly
NM_005431.1:c.19A>G NP_005422.1:p.Arg7Gly
NM_005431.2:c.19A>G MANE Select NP_005422.1:p.Arg7Gly
Search 100 bp 5'
Search 100 bp 3'