Canonical Allele Identifier: CA169486938
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1758441
ClinVar RCV Id: RCV002380237
dbSNP Id: rs749779141
MyVariant Identifiers: chr7:g.152345836T>A (hg19) chr7:g.152648751T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648751T>A , CM000669.2:g.152648751T>A GRCh38
NC_000007.13:g.152345836T>A , CM000669.1:g.152345836T>A GRCh37
NC_000007.12:g.151976769T>A NCBI36
NG_027988.1:g.32415A>T
NG_027988.2:g.32415A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.566A>T ENSP00000513758.1:p.Asp189Val
ENST00000359321.2:c.734A>T MANE Select ENSP00000352271.1:p.Asp245Val
ENST00000359321.1:c.734A>T ENSP00000352271.1:p.Asp245Val
ENST00000495707.1:n.756A>T
NM_005431.1:c.734A>T NP_005422.1:p.Asp245Val
NM_005431.2:c.734A>T MANE Select NP_005422.1:p.Asp245Val
Search 100 bp 5'
Search 100 bp 3'