Canonical Allele Identifier: CA370198169
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3224691
ClinVar RCV Id: RCV004521381
dbSNP Id: rs2098027173

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648798C>G , CM000669.2:g.152648798C>G GRCh38
NC_000007.13:g.152345883C>G , CM000669.1:g.152345883C>G GRCh37
NC_000007.12:g.151976816C>G NCBI36
NG_027988.1:g.32368G>C
NG_027988.2:g.32368G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.519G>C ENSP00000513758.1:p.Lys173Asn
ENST00000359321.2:c.687G>C MANE Select ENSP00000352271.1:p.Lys229Asn
ENST00000359321.1:c.687G>C ENSP00000352271.1:p.Lys229Asn
ENST00000495707.1:n.709G>C
NM_005431.1:c.687G>C NP_005422.1:p.Lys229Asn
NM_005431.2:c.687G>C MANE Select NP_005422.1:p.Lys229Asn