Canonical Allele Identifier: CA4582445
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2587622
ClinVar RCV Id: RCV003344147
dbSNP Id: rs781763823
ExAC: 7:152373132 C / T
gnomAD v2: 7-152373132-C-T
gnomAD v4: 7-152676047-C-T
MyVariant Identifiers: chr7:g.152373132C>T (hg19) chr7:g.152676047C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676047C>T , CM000669.2:g.152676047C>T GRCh38
NC_000007.13:g.152373132C>T , CM000669.1:g.152373132C>T GRCh37
NC_000007.12:g.152004065C>T NCBI36
NG_027988.1:g.5119G>A
NG_027988.2:g.5119G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-54G>A ENSP00000513758.1:n.-54G>A
ENST00000698507.1:n.101G>A
ENST00000359321.2:c.33G>A MANE Select ENSP00000352271.1:p.Gly11=
ENST00000359321.1:c.33G>A ENSP00000352271.1:p.Gly11=
NM_005431.1:c.33G>A NP_005422.1:p.Gly11=
NM_005431.2:c.33G>A MANE Select NP_005422.1:p.Gly11=
Search 100 bp 5'
Search 100 bp 3'