Canonical Allele Identifier: CA16605196
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 390485
ClinVar RCV Id: RCV000439235
dbSNP Id: rs1057523790
gnomAD v2: 7-152357778-T-C
gnomAD v4: 7-152660693-T-C
MyVariant Identifiers: chr7:g.152357778T>C (hg19) chr7:g.152660693T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660693T>C , CM000669.2:g.152660693T>C GRCh38
NC_000007.13:g.152357778T>C , CM000669.1:g.152357778T>C GRCh37
NC_000007.12:g.151988711T>C NCBI36
NG_027988.1:g.20473A>G
NG_027988.2:g.20473A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11330A>G ENSP00000513758.1:n.-47-11330A>G
ENST00000698507.1:n.197A>G
ENST00000359321.2:c.121+8A>G MANE Select ENSP00000352271.1:n.121+8A>G
ENST00000359321.1:c.121+8A>G ENSP00000352271.1:n.121+8A>G
ENST00000495707.1:n.143+8A>G
NM_005431.1:c.121+8A>G NP_005422.1:n.121+8A>G
NM_005431.2:c.121+8A>G MANE Select NP_005422.1:n.121+8A>G
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