Canonical Allele Identifier: CA2716215332
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2117014083
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675778A>C , CM000669.2:g.152675778A>C GRCh38
NC_000007.13:g.152372863A>C , CM000669.1:g.152372863A>C GRCh37
NC_000007.12:g.152003796A>C NCBI36
NG_027988.1:g.5388T>G
NG_027988.2:g.5388T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+263T>G ENSP00000513758.1:n.-48+263T>G
ENST00000698507.1:n.107+263T>G
ENST00000359321.2:c.39+263T>G MANE Select ENSP00000352271.1:n.39+263T>G
ENST00000359321.1:c.39+263T>G ENSP00000352271.1:n.39+263T>G
NM_005431.1:c.39+263T>G NP_005422.1:n.39+263T>G
NM_005431.2:c.39+263T>G MANE Select NP_005422.1:n.39+263T>G
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