Canonical Allele Identifier: CA370198922
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2447652
ClinVar RCV Id: RCV003167962
MyVariant Identifiers: chr7:g.152346235A>G (hg19) chr7:g.152649150A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649150A>G , CM000669.2:g.152649150A>G GRCh38
NC_000007.13:g.152346235A>G , CM000669.1:g.152346235A>G GRCh37
NC_000007.12:g.151977168A>G NCBI36
NG_027988.1:g.32016T>C
NG_027988.2:g.32016T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.167T>C ENSP00000513758.1:p.Leu56Pro
ENST00000359321.2:c.335T>C MANE Select ENSP00000352271.1:p.Leu112Pro
ENST00000359321.1:c.335T>C ENSP00000352271.1:p.Leu112Pro
ENST00000495707.1:n.357T>C
NM_005431.1:c.335T>C NP_005422.1:p.Leu112Pro
NM_005431.2:c.335T>C MANE Select NP_005422.1:p.Leu112Pro
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