Canonical Allele Identifier: CA1108867654
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1099536
ClinVar RCV Id: RCV001421851
dbSNP Id: rs2098040921
gnomAD v3: 7-152676032-G-A
gnomAD v4: 7-152676032-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676032G>A , CM000669.2:g.152676032G>A GRCh38
NC_000007.13:g.152373117G>A , CM000669.1:g.152373117G>A GRCh37
NC_000007.12:g.152004050G>A NCBI36
NG_027988.1:g.5134C>T
NG_027988.2:g.5134C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+9C>T ENSP00000513758.1:n.-48+9C>T
ENST00000698507.1:n.107+9C>T
ENST00000359321.2:c.39+9C>T MANE Select ENSP00000352271.1:n.39+9C>T
ENST00000359321.1:c.39+9C>T ENSP00000352271.1:n.39+9C>T
NM_005431.1:c.39+9C>T NP_005422.1:n.39+9C>T
NM_005431.2:c.39+9C>T MANE Select NP_005422.1:n.39+9C>T
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