Canonical Allele Identifier: CA4582444

Gene: XRCC2

Linked Data

• ClinVar Variation Id: 1034722
• ClinVar RCV Id: RCV001337487 ; RCV002357175
• dbSNP Id: rs373877121
• ExAC: 7:152373126 C / G
• gnomAD v2: 7-152373126-C-G
• gnomAD v3: 7-152676041-C-G
• gnomAD v4: 7-152676041-C-G
• MyVariant Identifiers: chr7:g.152373126C>G (hg19) ; chr7:g.152676041C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676041C>G , CM000669.2:g.152676041C>G	GRCh38
NC_000007.13:g.152373126C>G , CM000669.1:g.152373126C>G	GRCh37
NC_000007.12:g.152004059C>G	NCBI36
NG_027988.1:g.5125G>C
NG_027988.2:g.5125G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48G>C	ENSP00000513758.1:n.-48G>C
ENST00000698507.1:n.107G>C
ENST00000359321.2:c.39G>C MANE Select	ENSP00000352271.1:p.Glu13Asp
ENST00000359321.1:c.39G>C	ENSP00000352271.1:p.Glu13Asp
NM_005431.1:c.39G>C	NP_005422.1:p.Glu13Asp
NM_005431.2:c.39G>C MANE Select	NP_005422.1:p.Glu13Asp