Canonical Allele Identifier: CA1753246346
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648414A= , CM000669.2:g.152648414A= GRCh38
NC_000007.13:g.152345499A= , CM000669.1:g.152345499A= GRCh37
NC_000007.12:g.151976432A= NCBI36
NG_027988.1:g.32752T=
NG_027988.2:g.32752T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*228T= ENSP00000513758.1:n.*228T=
ENST00000359321.2:c.*228T= MANE Select ENSP00000352271.1:n.*228T=
ENST00000359321.1:c.*228T= ENSP00000352271.1:n.*228T=
ENST00000495707.1:n.1093T=
NM_005431.1:c.*228T= NP_005422.1:n.*228T=
NM_005431.2:c.*228T= MANE Select NP_005422.1:n.*228T=
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