Canonical Allele Identifier: CA1753256980
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660533C= , CM000669.2:g.152660533C= GRCh38
NC_000007.13:g.152357618C= , CM000669.1:g.152357618C= GRCh37
NC_000007.12:g.151988551C= NCBI36
NG_027988.1:g.20633G=
NG_027988.2:g.20633G=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11170G= ENSP00000513758.1:n.-47-11170G=
ENST00000698507.1:n.357G=
ENST00000359321.2:c.121+168G= MANE Select ENSP00000352271.1:n.121+168G=
ENST00000359321.1:c.121+168G= ENSP00000352271.1:n.121+168G=
ENST00000495707.1:n.143+168G=
NM_005431.1:c.121+168G= NP_005422.1:n.121+168G=
NM_005431.2:c.121+168G= MANE Select NP_005422.1:n.121+168G=
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