Canonical Allele Identifier: CA169488166
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs761120166
gnomAD v3: 7-152660533-C-T
gnomAD v4: 7-152660533-C-T
MyVariant Identifiers: chr7:g.152357618C>T (hg19) chr7:g.152660533C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660533C>T , CM000669.2:g.152660533C>T GRCh38
NC_000007.13:g.152357618C>T , CM000669.1:g.152357618C>T GRCh37
NC_000007.12:g.151988551C>T NCBI36
NG_027988.1:g.20633G>A
NG_027988.2:g.20633G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11170G>A ENSP00000513758.1:n.-47-11170G>A
ENST00000698507.1:n.357G>A
ENST00000359321.2:c.121+168G>A MANE Select ENSP00000352271.1:n.121+168G>A
ENST00000359321.1:c.121+168G>A ENSP00000352271.1:n.121+168G>A
ENST00000495707.1:n.143+168G>A
NM_005431.1:c.121+168G>A NP_005422.1:n.121+168G>A
NM_005431.2:c.121+168G>A MANE Select NP_005422.1:n.121+168G>A
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