Canonical Allele Identifier: CA4582309
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 826651
dbSNP Id: rs771722750

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648803A>G , CM000669.2:g.152648803A>G GRCh38
NC_000007.13:g.152345888A>G , CM000669.1:g.152345888A>G GRCh37
NC_000007.12:g.151976821A>G NCBI36
NG_027988.1:g.32363T>C
NG_027988.2:g.32363T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.514T>C ENSP00000513758.1:p.Cys172Arg
ENST00000359321.2:c.682T>C MANE Select ENSP00000352271.1:p.Cys228Arg
ENST00000359321.1:c.682T>C ENSP00000352271.1:p.Cys228Arg
ENST00000495707.1:n.704T>C
NM_005431.1:c.682T>C NP_005422.1:p.Cys228Arg
NM_005431.2:c.682T>C MANE Select NP_005422.1:p.Cys228Arg