Canonical Allele Identifier: CA1753246372
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648475C= , CM000669.2:g.152648475C= GRCh38
NC_000007.13:g.152345560C= , CM000669.1:g.152345560C= GRCh37
NC_000007.12:g.151976493C= NCBI36
NG_027988.1:g.32691G=
NG_027988.2:g.32691G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*167G= ENSP00000513758.1:n.*167G=
ENST00000359321.2:c.*167G= MANE Select ENSP00000352271.1:n.*167G=
ENST00000359321.1:c.*167G= ENSP00000352271.1:n.*167G=
ENST00000495707.1:n.1032G=
NM_005431.1:c.*167G= NP_005422.1:n.*167G=
NM_005431.2:c.*167G= MANE Select NP_005422.1:n.*167G=
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