Canonical Allele Identifier: CA169486914
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs981069834
gnomAD v2: 7-152345508-AAAAAAG-A
gnomAD v3: 7-152648423-AAAAAAG-A
gnomAD v4: 7-152648423-AAAAAAG-A
MyVariant Identifiers: chr7:g.152345509_152345514del (hg19) chr7:g.152648424_152648429del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648428_152648433del , CM000669.2:g.152648428_152648433del GRCh38
NC_000007.13:g.152345513_152345518del , CM000669.1:g.152345513_152345518del GRCh37
NC_000007.12:g.151976446_151976451del NCBI36
NG_027988.1:g.32737_32742del
NG_027988.2:g.32737_32742del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*213_*218del ENSP00000513758.1:n.*213_*218del
ENST00000359321.2:c.*213_*218del MANE Select ENSP00000352271.1:n.*213_*218del
ENST00000359321.1:c.*213_*218del ENSP00000352271.1:n.*213_*218del
ENST00000495707.1:n.1078_1083del
NM_005431.1:c.*213_*218del NP_005422.1:n.*213_*218del
NM_005431.2:c.*213_*218del MANE Select NP_005422.1:n.*213_*218del
Search 100 bp 5'
Search 100 bp 3'