Canonical Allele Identifier: CA431165607
Gene: XRCC5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr2:g.216986845C>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122122C>T , CM000664.2:g.216122122C>T GRCh38
NC_000002.11:g.216986845C>T , CM000664.1:g.216986845C>T GRCh37
NC_000002.10:g.216695090C>T NCBI36
NG_029780.1:g.17826C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.552C>T MANE Select ENSP00000375977.2:p.Arg184=
ENST00000392132.6:c.552C>T ENSP00000375977.2:p.Arg184=
ENST00000392133.7:c.552C>T ENSP00000375978.3:p.Arg184=
ENST00000460284.5:n.1094C>T
NM_021141.3:c.552C>T NP_066964.1:p.Arg184=
NM_021141.4:c.552C>T MANE Select NP_066964.1:p.Arg184=
Search 100 bp 5'
Search 100 bp 3'