Canonical Allele Identifier: CA350493340
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs764110781
MyVariant Identifiers: chr2:g.216986843C>A (hg19) chr2:g.216122120C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122120C>A , CM000664.2:g.216122120C>A GRCh38
NC_000002.11:g.216986843C>A , CM000664.1:g.216986843C>A GRCh37
NC_000002.10:g.216695088C>A NCBI36
NG_029780.1:g.17824C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.550C>A MANE Select ENSP00000375977.2:p.Arg184Ser
ENST00000392132.6:c.550C>A ENSP00000375977.2:p.Arg184Ser
ENST00000392133.7:c.550C>A ENSP00000375978.3:p.Arg184Ser
ENST00000460284.5:n.1092C>A
NM_021141.3:c.550C>A NP_066964.1:p.Arg184Ser
NM_021141.4:c.550C>A MANE Select NP_066964.1:p.Arg184Ser
Search 100 bp 5'
Search 100 bp 3'