Canonical Allele Identifier: CA4582434
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs192964346
ExAC: 7:152373103 A / G
gnomAD v2: 7-152373103-A-G
gnomAD v3: 7-152676018-A-G
gnomAD v4: 7-152676018-A-G
MyVariant Identifiers: chr7:g.152373103A>G (hg19) chr7:g.152676018A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676018A>G , CM000669.2:g.152676018A>G GRCh38
NC_000007.13:g.152373103A>G , CM000669.1:g.152373103A>G GRCh37
NC_000007.12:g.152004036A>G NCBI36
NG_027988.1:g.5148T>C
NG_027988.2:g.5148T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+23T>C ENSP00000513758.1:n.-48+23T>C
ENST00000698507.1:n.107+23T>C
ENST00000359321.2:c.39+23T>C MANE Select ENSP00000352271.1:n.39+23T>C
ENST00000359321.1:c.39+23T>C ENSP00000352271.1:n.39+23T>C
NM_005431.1:c.39+23T>C NP_005422.1:n.39+23T>C
NM_005431.2:c.39+23T>C MANE Select NP_005422.1:n.39+23T>C
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