Canonical Allele Identifier: CA370198064
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 826962
ClinVar RCV Id: RCV001026268 RCV003558645
dbSNP Id: rs1590129246
gnomAD v4: 7-152648754-T-C
MyVariant Identifiers: chr7:g.152345839T>C (hg19) chr7:g.152648754T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648754T>C , CM000669.2:g.152648754T>C GRCh38
NC_000007.13:g.152345839T>C , CM000669.1:g.152345839T>C GRCh37
NC_000007.12:g.151976772T>C NCBI36
NG_027988.1:g.32412A>G
NG_027988.2:g.32412A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.563A>G ENSP00000513758.1:p.Gln188Arg
ENST00000359321.2:c.731A>G MANE Select ENSP00000352271.1:p.Gln244Arg
ENST00000359321.1:c.731A>G ENSP00000352271.1:p.Gln244Arg
ENST00000495707.1:n.753A>G
NM_005431.1:c.731A>G NP_005422.1:p.Gln244Arg
NM_005431.2:c.731A>G MANE Select NP_005422.1:p.Gln244Arg
Search 100 bp 5'
Search 100 bp 3'