Canonical Allele Identifier: CA1753273957
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2098040560
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675577G>C , CM000669.2:g.152675577G>C GRCh38
NC_000007.13:g.152372662G>C , CM000669.1:g.152372662G>C GRCh37
NC_000007.12:g.152003595G>C NCBI36
NG_027988.1:g.5589C>G
NG_027988.2:g.5589C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+464C>G ENSP00000513758.1:n.-48+464C>G
ENST00000698507.1:n.107+464C>G
ENST00000359321.2:c.39+464C>G MANE Select ENSP00000352271.1:n.39+464C>G
ENST00000359321.1:c.39+464C>G ENSP00000352271.1:n.39+464C>G
NM_005431.1:c.39+464C>G NP_005422.1:n.39+464C>G
NM_005431.2:c.39+464C>G MANE Select NP_005422.1:n.39+464C>G
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