Canonical Allele Identifier: CA764677193
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1371345978
gnomAD v3: 2-216205555-G-C
gnomAD v4: 2-216205555-G-C
MyVariant Identifiers: chr2:g.217070278G>C (hg19) chr2:g.216205555G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205555G>C , CM000664.2:g.216205555G>C GRCh38
NC_000002.11:g.217070278G>C , CM000664.1:g.217070278G>C GRCh37
NC_000002.10:g.216778523G>C NCBI36
NG_029780.1:g.101259G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*353G>C MANE Select ENSP00000375977.2:n.*353G>C
ENST00000392132.6:c.*353G>C ENSP00000375977.2:n.*353G>C
ENST00000392133.7:c.*353G>C ENSP00000375978.3:n.*353G>C
NM_021141.3:c.*353G>C NP_066964.1:n.*353G>C
NM_021141.4:c.*353G>C MANE Select NP_066964.1:n.*353G>C
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