Canonical Allele Identifier: CA370199511
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152357841A>C (hg19) chr7:g.152660756A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660756A>C , CM000669.2:g.152660756A>C GRCh38
NC_000007.13:g.152357841A>C , CM000669.1:g.152357841A>C GRCh37
NC_000007.12:g.151988774A>C NCBI36
NG_027988.1:g.20410T>G
NG_027988.2:g.20410T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11393T>G ENSP00000513758.1:n.-47-11393T>G
ENST00000698507.1:n.134T>G
ENST00000359321.2:c.66T>G MANE Select ENSP00000352271.1:p.Ser22Arg
ENST00000359321.1:c.66T>G ENSP00000352271.1:p.Ser22Arg
ENST00000495707.1:n.88T>G
NM_005431.1:c.66T>G NP_005422.1:p.Ser22Arg
NM_005431.2:c.66T>G MANE Select NP_005422.1:p.Ser22Arg
Search 100 bp 5'
Search 100 bp 3'