Canonical Allele Identifier: CA539838338

Gene: XRCC5

Linked Data

• dbSNP Id: rs1383531364
• gnomAD v2: 2-216986770-G-C
• gnomAD v4: 2-216122047-G-C
• MyVariant Identifiers: chr2:g.216986770G>C (hg19) ; chr2:g.216122047G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.216122047G>C , CM000664.2:g.216122047G>C	GRCh38
NC_000002.11:g.216986770G>C , CM000664.1:g.216986770G>C	GRCh37
NC_000002.10:g.216695015G>C	NCBI36
NG_029780.1:g.17751G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000392132.7:c.492-15G>C MANE Select	ENSP00000375977.2:n.492-15G>C
ENST00000392132.6:c.492-15G>C	ENSP00000375977.2:n.492-15G>C
ENST00000392133.7:c.492-15G>C	ENSP00000375978.3:n.492-15G>C
ENST00000460284.5:n.1034-15G>C
NM_021141.3:c.492-15G>C	NP_066964.1:n.492-15G>C
NM_021141.4:c.492-15G>C MANE Select	NP_066964.1:n.492-15G>C