Canonical Allele Identifier: CA764677195
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1427913887
gnomAD v3: 2-216205564-G-A
gnomAD v4: 2-216205564-G-A
MyVariant Identifiers: chr2:g.217070287G>A (hg19) chr2:g.216205564G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205564G>A , CM000664.2:g.216205564G>A GRCh38
NC_000002.11:g.217070287G>A , CM000664.1:g.217070287G>A GRCh37
NC_000002.10:g.216778532G>A NCBI36
NG_029780.1:g.101268G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*362G>A MANE Select ENSP00000375977.2:n.*362G>A
ENST00000392132.6:c.*362G>A ENSP00000375977.2:n.*362G>A
ENST00000392133.7:c.*362G>A ENSP00000375978.3:n.*362G>A
NM_021141.3:c.*362G>A NP_066964.1:n.*362G>A
NM_021141.4:c.*362G>A MANE Select NP_066964.1:n.*362G>A
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