Canonical Allele Identifier: CA458895337
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1753636
ClinVar RCV Id: RCV002361879
dbSNP Id: rs1252484061
gnomAD v2: 7-152345925-T-G
gnomAD v4: 7-152648840-T-G
MyVariant Identifiers: chr7:g.152345925T>G (hg19) chr7:g.152648840T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648840T>G , CM000669.2:g.152648840T>G GRCh38
NC_000007.13:g.152345925T>G , CM000669.1:g.152345925T>G GRCh37
NC_000007.12:g.151976858T>G NCBI36
NG_027988.1:g.32326A>C
NG_027988.2:g.32326A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.477A>C ENSP00000513758.1:p.Arg159=
ENST00000359321.2:c.645A>C MANE Select ENSP00000352271.1:p.Arg215=
ENST00000359321.1:c.645A>C ENSP00000352271.1:p.Arg215=
ENST00000495707.1:n.667A>C
NM_005431.1:c.645A>C NP_005422.1:p.Arg215=
NM_005431.2:c.645A>C MANE Select NP_005422.1:p.Arg215=
Search 100 bp 5'
Search 100 bp 3'