Canonical Allele Identifier: CA458805213
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2619679
ClinVar RCV Id: RCV003383128
MyVariant Identifiers: chr7:g.152373132C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676047C>A , CM000669.2:g.152676047C>A GRCh38
NC_000007.13:g.152373132C>A , CM000669.1:g.152373132C>A GRCh37
NC_000007.12:g.152004065C>A NCBI36
NG_027988.1:g.5119G>T
NG_027988.2:g.5119G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-54G>T ENSP00000513758.1:n.-54G>T
ENST00000698507.1:n.101G>T
ENST00000359321.2:c.33G>T MANE Select ENSP00000352271.1:p.Gly11=
ENST00000359321.1:c.33G>T ENSP00000352271.1:p.Gly11=
NM_005431.1:c.33G>T NP_005422.1:p.Gly11=
NM_005431.2:c.33G>T MANE Select NP_005422.1:p.Gly11=
Search 100 bp 5'
Search 100 bp 3'