Canonical Allele Identifier: CA1753257116
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660686G= , CM000669.2:g.152660686G= GRCh38
NC_000007.13:g.152357771G= , CM000669.1:g.152357771G= GRCh37
NC_000007.12:g.151988704G= NCBI36
NG_027988.1:g.20480C=
NG_027988.2:g.20480C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11323C= ENSP00000513758.1:n.-47-11323C=
ENST00000698507.1:n.204C=
ENST00000359321.2:c.121+15C= MANE Select ENSP00000352271.1:n.121+15C=
ENST00000359321.1:c.121+15C= ENSP00000352271.1:n.121+15C=
ENST00000495707.1:n.143+15C=
NM_005431.1:c.121+15C= NP_005422.1:n.121+15C=
NM_005431.2:c.121+15C= MANE Select NP_005422.1:n.121+15C=
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