Canonical Allele Identifier: CA169488168
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs923908876
MyVariant Identifiers: chr7:g.152357627A>G (hg19) chr7:g.152660542A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660542A>G , CM000669.2:g.152660542A>G GRCh38
NC_000007.13:g.152357627A>G , CM000669.1:g.152357627A>G GRCh37
NC_000007.12:g.151988560A>G NCBI36
NG_027988.1:g.20624T>C
NG_027988.2:g.20624T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11179T>C ENSP00000513758.1:n.-47-11179T>C
ENST00000698507.1:n.348T>C
ENST00000359321.2:c.121+159T>C MANE Select ENSP00000352271.1:n.121+159T>C
ENST00000359321.1:c.121+159T>C ENSP00000352271.1:n.121+159T>C
ENST00000495707.1:n.143+159T>C
NM_005431.1:c.121+159T>C NP_005422.1:n.121+159T>C
NM_005431.2:c.121+159T>C MANE Select NP_005422.1:n.121+159T>C
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