Canonical Allele Identifier: CA458805234
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1796183
ClinVar RCV Id: RCV002441557
dbSNP Id: rs1339516564
gnomAD v2: 7-152373138-C-T
gnomAD v4: 7-152676053-C-T
MyVariant Identifiers: chr7:g.152373138C>T (hg19) chr7:g.152676053C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676053C>T , CM000669.2:g.152676053C>T GRCh38
NC_000007.13:g.152373138C>T , CM000669.1:g.152373138C>T GRCh37
NC_000007.12:g.152004071C>T NCBI36
NG_027988.1:g.5113G>A
NG_027988.2:g.5113G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-60G>A ENSP00000513758.1:n.-60G>A
ENST00000698507.1:n.95G>A
ENST00000359321.2:c.27G>A MANE Select ENSP00000352271.1:p.Glu9=
ENST00000359321.1:c.27G>A ENSP00000352271.1:p.Glu9=
NM_005431.1:c.27G>A NP_005422.1:p.Glu9=
NM_005431.2:c.27G>A MANE Select NP_005422.1:p.Glu9=
Search 100 bp 5'
Search 100 bp 3'