Canonical Allele Identifier: CA764677199
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs1248549056
MyVariant Identifiers: chr2:g.217070290T>C (hg19) chr2:g.216205567T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216205567T>C , CM000664.2:g.216205567T>C GRCh38
NC_000002.11:g.217070290T>C , CM000664.1:g.217070290T>C GRCh37
NC_000002.10:g.216778535T>C NCBI36
NG_029780.1:g.101271T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.*365T>C MANE Select ENSP00000375977.2:n.*365T>C
ENST00000392132.6:c.*365T>C ENSP00000375977.2:n.*365T>C
ENST00000392133.7:c.*365T>C ENSP00000375978.3:n.*365T>C
NM_021141.3:c.*365T>C NP_066964.1:n.*365T>C
NM_021141.4:c.*365T>C MANE Select NP_066964.1:n.*365T>C
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