Canonical Allele Identifier: CA835365291
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1447886474
gnomAD v3: 7-152675664-AG-A
gnomAD v4: 7-152675664-AG-A
MyVariant Identifiers: chr7:g.152372750del (hg19) chr7:g.152675665del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675665del , CM000669.2:g.152675665del GRCh38
NC_000007.13:g.152372750del , CM000669.1:g.152372750del GRCh37
NC_000007.12:g.152003683del NCBI36
NG_027988.1:g.5501del
NG_027988.2:g.5501del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+376del ENSP00000513758.1:n.-48+376del
ENST00000698507.1:n.107+376del
ENST00000359321.2:c.39+376del MANE Select ENSP00000352271.1:n.39+376del
ENST00000359321.1:c.39+376del ENSP00000352271.1:n.39+376del
NM_005431.1:c.39+376del NP_005422.1:n.39+376del
NM_005431.2:c.39+376del MANE Select NP_005422.1:n.39+376del
Search 100 bp 5'
Search 100 bp 3'