Canonical Allele Identifier: CA2685736305
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152660593-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660593T>G , CM000669.2:g.152660593T>G GRCh38
NC_000007.13:g.152357678T>G , CM000669.1:g.152357678T>G GRCh37
NC_000007.12:g.151988611T>G NCBI36
NG_027988.1:g.20573A>C
NG_027988.2:g.20573A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11230A>C ENSP00000513758.1:n.-47-11230A>C
ENST00000698507.1:n.297A>C
ENST00000359321.2:c.121+108A>C MANE Select ENSP00000352271.1:n.121+108A>C
ENST00000359321.1:c.121+108A>C ENSP00000352271.1:n.121+108A>C
ENST00000495707.1:n.143+108A>C
NM_005431.1:c.121+108A>C NP_005422.1:n.121+108A>C
NM_005431.2:c.121+108A>C MANE Select NP_005422.1:n.121+108A>C
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