Canonical Allele Identifier: CA2096679
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs780385135
ExAC: 2:216986735 G / A
gnomAD v2: 2-216986735-G-A
gnomAD v4: 2-216122012-G-A
MyVariant Identifiers: chr2:g.216986735G>A (hg19) chr2:g.216122012G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216122012G>A , CM000664.2:g.216122012G>A GRCh38
NC_000002.11:g.216986735G>A , CM000664.1:g.216986735G>A GRCh37
NC_000002.10:g.216694980G>A NCBI36
NG_029780.1:g.17716G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.492-50G>A MANE Select ENSP00000375977.2:n.492-50G>A
ENST00000392132.6:c.492-50G>A ENSP00000375977.2:n.492-50G>A
ENST00000392133.7:c.492-50G>A ENSP00000375978.3:n.492-50G>A
ENST00000460284.5:n.1034-50G>A
NM_021141.3:c.492-50G>A NP_066964.1:n.492-50G>A
NM_021141.4:c.492-50G>A MANE Select NP_066964.1:n.492-50G>A
Search 100 bp 5'
Search 100 bp 3'