Canonical Allele Identifier: CA4582393
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs781325306
ExAC: 7:152357756 AT / A
gnomAD v2: 7-152357756-AT-A
gnomAD v3: 7-152660671-AT-A
gnomAD v4: 7-152660671-AT-A
MyVariant Identifiers: chr7:g.152357757del (hg19) chr7:g.152660672del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660674del , CM000669.2:g.152660674del GRCh38
NC_000007.13:g.152357759del , CM000669.1:g.152357759del GRCh37
NC_000007.12:g.151988692del NCBI36
NG_027988.1:g.20494del
NG_027988.2:g.20494del

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11309del ENSP00000513758.1:n.-47-11309del
ENST00000698507.1:n.218del
ENST00000359321.2:c.121+29del MANE Select ENSP00000352271.1:n.121+29del
ENST00000359321.1:c.121+29del ENSP00000352271.1:n.121+29del
ENST00000495707.1:n.143+29del
NM_005431.1:c.121+29del NP_005422.1:n.121+29del
NM_005431.2:c.121+29del MANE Select NP_005422.1:n.121+29del
Search 100 bp 5'
Search 100 bp 3'