Canonical Allele Identifier: CA835376666
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1239379942
gnomAD v3: 7-152648400-A-C
gnomAD v4: 7-152648400-A-C
MyVariant Identifiers: chr7:g.152345485A>C (hg19) chr7:g.152648400A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648400A>C , CM000669.2:g.152648400A>C GRCh38
NC_000007.13:g.152345485A>C , CM000669.1:g.152345485A>C GRCh37
NC_000007.12:g.151976418A>C NCBI36
NG_027988.1:g.32766T>G
NG_027988.2:g.32766T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*242T>G ENSP00000513758.1:n.*242T>G
ENST00000359321.2:c.*242T>G MANE Select ENSP00000352271.1:n.*242T>G
ENST00000359321.1:c.*242T>G ENSP00000352271.1:n.*242T>G
ENST00000495707.1:n.1107T>G
NM_005431.1:c.*242T>G NP_005422.1:n.*242T>G
NM_005431.2:c.*242T>G MANE Select NP_005422.1:n.*242T>G
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