Canonical Allele Identifier: CA370198282
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1752827
ClinVar RCV Id: RCV002368855
MyVariant Identifiers: chr7:g.152345939G>C (hg19) chr7:g.152648854G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648854G>C , CM000669.2:g.152648854G>C GRCh38
NC_000007.13:g.152345939G>C , CM000669.1:g.152345939G>C GRCh37
NC_000007.12:g.151976872G>C NCBI36
NG_027988.1:g.32312C>G
NG_027988.2:g.32312C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.463C>G ENSP00000513758.1:p.His155Asp
ENST00000359321.2:c.631C>G MANE Select ENSP00000352271.1:p.His211Asp
ENST00000359321.1:c.631C>G ENSP00000352271.1:p.His211Asp
ENST00000495707.1:n.653C>G
NM_005431.1:c.631C>G NP_005422.1:p.His211Asp
NM_005431.2:c.631C>G MANE Select NP_005422.1:p.His211Asp
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