Canonical Allele Identifier: CA4582442
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 421370
ClinVar RCV Id: RCV001021395
dbSNP Id: rs560785131

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676040C>T , CM000669.2:g.152676040C>T GRCh38
NC_000007.13:g.152373125C>T , CM000669.1:g.152373125C>T GRCh37
NC_000007.12:g.152004058C>T NCBI36
NG_027988.1:g.5126G>A
NG_027988.2:g.5126G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-48+1G>A ENSP00000513758.1:n.-48+1G>A
ENST00000698507.1:n.107+1G>A
ENST00000359321.2:c.39+1G>A MANE Select ENSP00000352271.1:n.39+1G>A
ENST00000359321.1:c.39+1G>A ENSP00000352271.1:n.39+1G>A
NM_005431.1:c.39+1G>A NP_005422.1:n.39+1G>A
NM_005431.2:c.39+1G>A MANE Select NP_005422.1:n.39+1G>A