Canonical Allele Identifier: CA65603074
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1026467973
gnomAD v2: 2-216986744-A-G
MyVariant Identifiers: chr2:g.216986744A>G (hg19) chr2:g.216122021A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122021A>G , CM000664.2:g.216122021A>G GRCh38
NC_000002.11:g.216986744A>G , CM000664.1:g.216986744A>G GRCh37
NC_000002.10:g.216694989A>G NCBI36
NG_029780.1:g.17725A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-41A>G MANE Select ENSP00000375977.2:n.492-41A>G
ENST00000392132.6:c.492-41A>G ENSP00000375977.2:n.492-41A>G
ENST00000392133.7:c.492-41A>G ENSP00000375978.3:n.492-41A>G
ENST00000460284.5:n.1034-41A>G
NM_021141.3:c.492-41A>G NP_066964.1:n.492-41A>G
NM_021141.4:c.492-41A>G MANE Select NP_066964.1:n.492-41A>G
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