Canonical Allele Identifier: CA4582441
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 824360
ClinVar RCV Id: RCV001021396 RCV001341372
dbSNP Id: rs758499439
ExAC: 7:152373124 A / T
gnomAD v2: 7-152373124-A-T
gnomAD v3: 7-152676039-A-T
gnomAD v4: 7-152676039-A-T
MyVariant Identifiers: chr7:g.152373124A>T (hg19) chr7:g.152676039A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676039A>T , CM000669.2:g.152676039A>T GRCh38
NC_000007.13:g.152373124A>T , CM000669.1:g.152373124A>T GRCh37
NC_000007.12:g.152004057A>T NCBI36
NG_027988.1:g.5127T>A
NG_027988.2:g.5127T>A

Transcript Alleles

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