Canonical Allele Identifier: CA16605309
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 387865
ClinVar RCV Id: RCV000421271 RCV002522401
dbSNP Id: rs1057522924
gnomAD v2: 7-152373114-G-A
gnomAD v4: 7-152676029-G-A
MyVariant Identifiers: chr7:g.152373114G>A (hg19) chr7:g.152676029G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676029G>A , CM000669.2:g.152676029G>A GRCh38
NC_000007.13:g.152373114G>A , CM000669.1:g.152373114G>A GRCh37
NC_000007.12:g.152004047G>A NCBI36
NG_027988.1:g.5137C>T
NG_027988.2:g.5137C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+12C>T ENSP00000513758.1:n.-48+12C>T
ENST00000698507.1:n.107+12C>T
ENST00000359321.2:c.39+12C>T MANE Select ENSP00000352271.1:n.39+12C>T
ENST00000359321.1:c.39+12C>T ENSP00000352271.1:n.39+12C>T
NM_005431.1:c.39+12C>T NP_005422.1:n.39+12C>T
NM_005431.2:c.39+12C>T MANE Select NP_005422.1:n.39+12C>T
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