Canonical Allele Identifier: CA370199586
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2166428
ClinVar RCV Id: RCV003080077
MyVariant Identifiers: chr7:g.152373134C>T (hg19) chr7:g.152676049C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676049C>T , CM000669.2:g.152676049C>T GRCh38
NC_000007.13:g.152373134C>T , CM000669.1:g.152373134C>T GRCh37
NC_000007.12:g.152004067C>T NCBI36
NG_027988.1:g.5117G>A
NG_027988.2:g.5117G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-56G>A ENSP00000513758.1:n.-56G>A
ENST00000698507.1:n.99G>A
ENST00000359321.2:c.31G>A MANE Select ENSP00000352271.1:p.Gly11Arg
ENST00000359321.1:c.31G>A ENSP00000352271.1:p.Gly11Arg
NM_005431.1:c.31G>A NP_005422.1:p.Gly11Arg
NM_005431.2:c.31G>A MANE Select NP_005422.1:p.Gly11Arg
Search 100 bp 5'
Search 100 bp 3'