Canonical Allele Identifier: CA2685735564
Gene: XRCC2 HGNC NCBI

Linked Data

gnomAD v4: 7-152648436-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648436T>G , CM000669.2:g.152648436T>G GRCh38
NC_000007.13:g.152345521T>G , CM000669.1:g.152345521T>G GRCh37
NC_000007.12:g.151976454T>G NCBI36
NG_027988.1:g.32730A>C
NG_027988.2:g.32730A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*206A>C ENSP00000513758.1:n.*206A>C
ENST00000359321.2:c.*206A>C MANE Select ENSP00000352271.1:n.*206A>C
ENST00000359321.1:c.*206A>C ENSP00000352271.1:n.*206A>C
ENST00000495707.1:n.1071A>C
NM_005431.1:c.*206A>C NP_005422.1:n.*206A>C
NM_005431.2:c.*206A>C MANE Select NP_005422.1:n.*206A>C
Search 100 bp 5'
Search 100 bp 3'