Canonical Allele Identifier: CA1753273991
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675599T= , CM000669.2:g.152675599T= GRCh38
NC_000007.13:g.152372684T= , CM000669.1:g.152372684T= GRCh37
NC_000007.12:g.152003617T= NCBI36
NG_027988.1:g.5567A=
NG_027988.2:g.5567A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+442A= ENSP00000513758.1:n.-48+442A=
ENST00000698507.1:n.107+442A=
ENST00000359321.2:c.39+442A= MANE Select ENSP00000352271.1:n.39+442A=
ENST00000359321.1:c.39+442A= ENSP00000352271.1:n.39+442A=
NM_005431.1:c.39+442A= NP_005422.1:n.39+442A=
NM_005431.2:c.39+442A= MANE Select NP_005422.1:n.39+442A=
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