Canonical Allele Identifier: CA458895257
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1226430
ClinVar RCV Id: RCV001615695
dbSNP Id: rs2116987114
gnomAD v4: 7-152648759-G-A
COSMIC: COSM3636564
MyVariant Identifiers: chr7:g.152345844G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648759G>A , CM000669.2:g.152648759G>A GRCh38
NC_000007.13:g.152345844G>A , CM000669.1:g.152345844G>A GRCh37
NC_000007.12:g.151976777G>A NCBI36
NG_027988.1:g.32407C>T
NG_027988.2:g.32407C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.558C>T ENSP00000513758.1:p.Ser186=
ENST00000359321.2:c.726C>T MANE Select ENSP00000352271.1:p.Ser242=
ENST00000359321.1:c.726C>T ENSP00000352271.1:p.Ser242=
ENST00000495707.1:n.748C>T
NM_005431.1:c.726C>T NP_005422.1:p.Ser242=
NM_005431.2:c.726C>T MANE Select NP_005422.1:p.Ser242=
Search 100 bp 5'
Search 100 bp 3'