Canonical Allele Identifier: CA764653733

Gene: XRCC5

Linked Data

• dbSNP Id: rs1208365556
• MyVariant Identifiers: chr2:g.216986721C>T (hg19) ; chr2:g.216121998C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216121998C>T , CM000664.2:g.216121998C>T	GRCh38
NC_000002.11:g.216986721C>T , CM000664.1:g.216986721C>T	GRCh37
NC_000002.10:g.216694966C>T	NCBI36
NG_029780.1:g.17702C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392132.7:c.492-64C>T MANE Select	ENSP00000375977.2:n.492-64C>T
ENST00000392132.6:c.492-64C>T	ENSP00000375977.2:n.492-64C>T
ENST00000392133.7:c.492-64C>T	ENSP00000375978.3:n.492-64C>T
ENST00000460284.5:n.1034-64C>T
NM_021141.3:c.492-64C>T	NP_066964.1:n.492-64C>T
NM_021141.4:c.492-64C>T MANE Select	NP_066964.1:n.492-64C>T