Canonical Allele Identifier: CA1753246369
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648463G= , CM000669.2:g.152648463G= GRCh38
NC_000007.13:g.152345548G= , CM000669.1:g.152345548G= GRCh37
NC_000007.12:g.151976481G= NCBI36
NG_027988.1:g.32703C=
NG_027988.2:g.32703C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*179C= ENSP00000513758.1:n.*179C=
ENST00000359321.2:c.*179C= MANE Select ENSP00000352271.1:n.*179C=
ENST00000359321.1:c.*179C= ENSP00000352271.1:n.*179C=
ENST00000495707.1:n.1044C=
NM_005431.1:c.*179C= NP_005422.1:n.*179C=
NM_005431.2:c.*179C= MANE Select NP_005422.1:n.*179C=
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