Canonical Allele Identifier: CA458895608
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1730714
ClinVar RCV Id: RCV002451723
gnomAD v4: 7-152649149-C-T
MyVariant Identifiers: chr7:g.152346234C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649149C>T , CM000669.2:g.152649149C>T GRCh38
NC_000007.13:g.152346234C>T , CM000669.1:g.152346234C>T GRCh37
NC_000007.12:g.151977167C>T NCBI36
NG_027988.1:g.32017G>A
NG_027988.2:g.32017G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.168G>A ENSP00000513758.1:p.Leu56=
ENST00000359321.2:c.336G>A MANE Select ENSP00000352271.1:p.Leu112=
ENST00000359321.1:c.336G>A ENSP00000352271.1:p.Leu112=
ENST00000495707.1:n.358G>A
NM_005431.1:c.336G>A NP_005422.1:p.Leu112=
NM_005431.2:c.336G>A MANE Select NP_005422.1:p.Leu112=
Search 100 bp 5'
Search 100 bp 3'