Canonical Allele Identifier: CA915945587
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 636233
ClinVar RCV Id: RCV000787936 RCV003307419
dbSNP Id: rs1590129294
gnomAD v4: 7-152648807-A-AT
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648808dup , CM000669.2:g.152648808dup GRCh38
NC_000007.13:g.152345893dup , CM000669.1:g.152345893dup GRCh37
NC_000007.12:g.151976826dup NCBI36
NG_027988.1:g.32358dup
NG_027988.2:g.32358dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.509dup ENSP00000513758.1:p.Tyr170Ter
ENST00000359321.2:c.677dup MANE Select ENSP00000352271.1:p.Tyr226Ter
ENST00000359321.1:c.677dup ENSP00000352271.1:p.Tyr226Ter
ENST00000495707.1:n.699dup
NM_005431.1:c.677dup NP_005422.1:p.Tyr226Ter
NM_005431.2:c.677dup MANE Select NP_005422.1:p.Tyr226Ter
Search 100 bp 5'
Search 100 bp 3'