Canonical Allele Identifier: CA1753256986
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

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