Canonical Allele Identifier: CA169486925
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs532040586
gnomAD v3: 7-152648475-C-T
gnomAD v4: 7-152648475-C-T
MyVariant Identifiers: chr7:g.152345560C>T (hg19) chr7:g.152648475C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648475C>T , CM000669.2:g.152648475C>T GRCh38
NC_000007.13:g.152345560C>T , CM000669.1:g.152345560C>T GRCh37
NC_000007.12:g.151976493C>T NCBI36
NG_027988.1:g.32691G>A
NG_027988.2:g.32691G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*167G>A ENSP00000513758.1:n.*167G>A
ENST00000359321.2:c.*167G>A MANE Select ENSP00000352271.1:n.*167G>A
ENST00000359321.1:c.*167G>A ENSP00000352271.1:n.*167G>A
ENST00000495707.1:n.1032G>A
NM_005431.1:c.*167G>A NP_005422.1:n.*167G>A
NM_005431.2:c.*167G>A MANE Select NP_005422.1:n.*167G>A
Search 100 bp 5'
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