Canonical Allele Identifier: CA169486907
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs370785819
gnomAD v2: 7-152345497-AG-A
gnomAD v3: 7-152648412-AG-A
gnomAD v4: 7-152648412-AG-A
MyVariant Identifiers: chr7:g.152345498del (hg19) chr7:g.152648413del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648413del , CM000669.2:g.152648413del GRCh38
NC_000007.13:g.152345498del , CM000669.1:g.152345498del GRCh37
NC_000007.12:g.151976431del NCBI36
NG_027988.1:g.32753del
NG_027988.2:g.32753del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*229del ENSP00000513758.1:n.*229del
ENST00000359321.2:c.*229del MANE Select ENSP00000352271.1:n.*229del
ENST00000359321.1:c.*229del ENSP00000352271.1:n.*229del
ENST00000495707.1:n.1094del
NM_005431.1:c.*229del NP_005422.1:n.*229del
NM_005431.2:c.*229del MANE Select NP_005422.1:n.*229del
Search 100 bp 5'
Search 100 bp 3'