Canonical Allele Identifier: CA65562530
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs764359193
gnomAD v2: 2-217070381-T-G
gnomAD v3: 2-216205658-T-G
gnomAD v4: 2-216205658-T-G
MyVariant Identifiers: chr2:g.217070381T>G (hg19) chr2:g.216205658T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205658T>G , CM000664.2:g.216205658T>G GRCh38
NC_000002.11:g.217070381T>G , CM000664.1:g.217070381T>G GRCh37
NC_000002.10:g.216778626T>G NCBI36
NG_029780.1:g.101362T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*456T>G MANE Select ENSP00000375977.2:n.*456T>G
ENST00000392132.6:c.*456T>G ENSP00000375977.2:n.*456T>G
ENST00000392133.7:c.*456T>G ENSP00000375978.3:n.*456T>G
NM_021141.3:c.*456T>G NP_066964.1:n.*456T>G
NM_021141.4:c.*456T>G MANE Select NP_066964.1:n.*456T>G
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