Canonical Allele Identifier: CA431159930
Gene: XRCC5 HGNC NCBI

Linked Data

dbSNP Id: rs207906
MyVariant Identifiers: chr2:g.217012901A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.216148178A>T , CM000664.2:g.216148178A>T GRCh38
NC_000002.11:g.217012901A>T , CM000664.1:g.217012901A>T GRCh37
NC_000002.10:g.216721146A>T NCBI36
NG_029780.1:g.43882A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000392132.7:c.1572A>T MANE Select ENSP00000375977.2:p.Thr524=
ENST00000392132.6:c.1572A>T ENSP00000375977.2:p.Thr524=
ENST00000392133.7:c.1572A>T ENSP00000375978.3:p.Thr524=
ENST00000460284.5:n.2114A>T
NM_021141.3:c.1572A>T NP_066964.1:p.Thr524=
NM_021141.4:c.1572A>T MANE Select NP_066964.1:p.Thr524=