Canonical Allele Identifier: CA370198458
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1747731
ClinVar RCV Id: RCV002349783
COSMIC: COSM354575
MyVariant Identifiers: chr7:g.152346024C>A (hg19) chr7:g.152648939C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648939C>A , CM000669.2:g.152648939C>A GRCh38
NC_000007.13:g.152346024C>A , CM000669.1:g.152346024C>A GRCh37
NC_000007.12:g.151976957C>A NCBI36
NG_027988.1:g.32227G>T
NG_027988.2:g.32227G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.378G>T ENSP00000513758.1:p.Lys126Asn
ENST00000359321.2:c.546G>T MANE Select ENSP00000352271.1:p.Lys182Asn
ENST00000359321.1:c.546G>T ENSP00000352271.1:p.Lys182Asn
ENST00000495707.1:n.568G>T
NM_005431.1:c.546G>T NP_005422.1:p.Lys182Asn
NM_005431.2:c.546G>T MANE Select NP_005422.1:p.Lys182Asn
Search 100 bp 5'
Search 100 bp 3'