Canonical Allele Identifier: CA578933276
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs10707642
gnomAD v2: 7-152345498-G-GA
gnomAD v3: 7-152648413-G-GA
gnomAD v4: 7-152648413-G-GA
MyVariant Identifiers: chr7:g.152345502_152345503insA (hg19) chr7:g.152345498_152345499insA (hg19) chr7:g.152648417_152648418insA (hg38) chr7:g.152648413_152648414insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648428dup , CM000669.2:g.152648428dup GRCh38
NC_000007.13:g.152345513dup , CM000669.1:g.152345513dup GRCh37
NC_000007.12:g.151976446dup NCBI36
NG_027988.1:g.32752dup
NG_027988.2:g.32752dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*228dup ENSP00000513758.1:n.*228dup
ENST00000359321.2:c.*228dup MANE Select ENSP00000352271.1:n.*228dup
ENST00000359321.1:c.*228dup ENSP00000352271.1:n.*228dup
ENST00000495707.1:n.1093dup
NM_005431.1:c.*228dup NP_005422.1:n.*228dup
NM_005431.2:c.*228dup MANE Select NP_005422.1:n.*228dup
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