Canonical Allele Identifier: CA1108857321
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1590129003
gnomAD v3: 7-152648396-T-G
gnomAD v4: 7-152648396-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648396T>G , CM000669.2:g.152648396T>G GRCh38
NC_000007.13:g.152345481T>G , CM000669.1:g.152345481T>G GRCh37
NC_000007.12:g.151976414T>G NCBI36
NG_027988.1:g.32770A>C
NG_027988.2:g.32770A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*246A>C ENSP00000513758.1:n.*246A>C
ENST00000359321.2:c.*246A>C MANE Select ENSP00000352271.1:n.*246A>C
ENST00000359321.1:c.*246A>C ENSP00000352271.1:n.*246A>C
ENST00000495707.1:n.1111A>C
NM_005431.1:c.*246A>C NP_005422.1:n.*246A>C
NM_005431.2:c.*246A>C MANE Select NP_005422.1:n.*246A>C
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