Canonical Allele Identifier: CA1753273971
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675591A= , CM000669.2:g.152675591A= GRCh38
NC_000007.13:g.152372676A= , CM000669.1:g.152372676A= GRCh37
NC_000007.12:g.152003609A= NCBI36
NG_027988.1:g.5575T=
NG_027988.2:g.5575T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+450T= ENSP00000513758.1:n.-48+450T=
ENST00000698507.1:n.107+450T=
ENST00000359321.2:c.39+450T= MANE Select ENSP00000352271.1:n.39+450T=
ENST00000359321.1:c.39+450T= ENSP00000352271.1:n.39+450T=
NM_005431.1:c.39+450T= NP_005422.1:n.39+450T=
NM_005431.2:c.39+450T= MANE Select NP_005422.1:n.39+450T=
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