Canonical Allele Identifier: CA169489718
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs370903842
gnomAD v3: 7-152675588-G-T
gnomAD v4: 7-152675588-G-T
MyVariant Identifiers: chr7:g.152372673G>T (hg19) chr7:g.152675588G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675588G>T , CM000669.2:g.152675588G>T GRCh38
NC_000007.13:g.152372673G>T , CM000669.1:g.152372673G>T GRCh37
NC_000007.12:g.152003606G>T NCBI36
NG_027988.1:g.5578C>A
NG_027988.2:g.5578C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+453C>A ENSP00000513758.1:n.-48+453C>A
ENST00000698507.1:n.107+453C>A
ENST00000359321.2:c.39+453C>A MANE Select ENSP00000352271.1:n.39+453C>A
ENST00000359321.1:c.39+453C>A ENSP00000352271.1:n.39+453C>A
NM_005431.1:c.39+453C>A NP_005422.1:n.39+453C>A
NM_005431.2:c.39+453C>A MANE Select NP_005422.1:n.39+453C>A
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