Canonical Allele Identifier: CA458805221
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 753320
ClinVar RCV Id: RCV000930546 RCV002320109
dbSNP Id: rs1590140912
MyVariant Identifiers: chr7:g.152373135A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676050A>G , CM000669.2:g.152676050A>G GRCh38
NC_000007.13:g.152373135A>G , CM000669.1:g.152373135A>G GRCh37
NC_000007.12:g.152004068A>G NCBI36
NG_027988.1:g.5116T>C
NG_027988.2:g.5116T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-57T>C ENSP00000513758.1:n.-57T>C
ENST00000698507.1:n.98T>C
ENST00000359321.2:c.30T>C MANE Select ENSP00000352271.1:p.Ser10=
ENST00000359321.1:c.30T>C ENSP00000352271.1:p.Ser10=
NM_005431.1:c.30T>C NP_005422.1:p.Ser10=
NM_005431.2:c.30T>C MANE Select NP_005422.1:p.Ser10=
Search 100 bp 5'
Search 100 bp 3'