Canonical Allele Identifier: CA2605671148
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2116986525
gnomAD v3: 7-152648397-A-G
gnomAD v4: 7-152648397-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648397A>G , CM000669.2:g.152648397A>G GRCh38
NC_000007.13:g.152345482A>G , CM000669.1:g.152345482A>G GRCh37
NC_000007.12:g.151976415A>G NCBI36
NG_027988.1:g.32769T>C
NG_027988.2:g.32769T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*245T>C ENSP00000513758.1:n.*245T>C
ENST00000359321.2:c.*245T>C MANE Select ENSP00000352271.1:n.*245T>C
ENST00000359321.1:c.*245T>C ENSP00000352271.1:n.*245T>C
ENST00000495707.1:n.1110T>C
NM_005431.1:c.*245T>C NP_005422.1:n.*245T>C
NM_005431.2:c.*245T>C MANE Select NP_005422.1:n.*245T>C
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