Canonical Allele Identifier: CA2685736363

Gene: XRCC2

Linked Data

• dbSNP Id: rs1064794394
• gnomAD v4: 7-152660692-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660698del , CM000669.2:g.152660698del	GRCh38
NC_000007.13:g.152357783del , CM000669.1:g.152357783del	GRCh37
NC_000007.12:g.151988716del	NCBI36
NG_027988.1:g.20473del
NG_027988.2:g.20473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-47-11330del	ENSP00000513758.1:n.-47-11330del
ENST00000698507.1:n.197del
ENST00000359321.2:c.121+8del MANE Select	ENSP00000352271.1:n.121+8del
ENST00000359321.1:c.121+8del	ENSP00000352271.1:n.121+8del
ENST00000495707.1:n.143+8del
NM_005431.1:c.121+8del	NP_005422.1:n.121+8del
NM_005431.2:c.121+8del MANE Select	NP_005422.1:n.121+8del