Canonical Allele Identifier: CA2663022301
Gene: XRCC5 HGNC NCBI

Linked Data

gnomAD v4: 2-216122028-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122028T>G , CM000664.2:g.216122028T>G GRCh38
NC_000002.11:g.216986751T>G , CM000664.1:g.216986751T>G GRCh37
NC_000002.10:g.216694996T>G NCBI36
NG_029780.1:g.17732T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-34T>G MANE Select ENSP00000375977.2:n.492-34T>G
ENST00000392132.6:c.492-34T>G ENSP00000375977.2:n.492-34T>G
ENST00000392133.7:c.492-34T>G ENSP00000375978.3:n.492-34T>G
ENST00000460284.5:n.1034-34T>G
NM_021141.3:c.492-34T>G NP_066964.1:n.492-34T>G
NM_021141.4:c.492-34T>G MANE Select NP_066964.1:n.492-34T>G
Search 100 bp 5'
Search 100 bp 3'