Canonical Allele Identifier: CA1753246420

Gene: XRCC2

Linked Data

• dbSNP Id: rs2098027028
• gnomAD v4: 7-152648560-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648563del , CM000669.2:g.152648563del	GRCh38
NC_000007.13:g.152345648del , CM000669.1:g.152345648del	GRCh37
NC_000007.12:g.151976581del	NCBI36
NG_027988.1:g.32605del
NG_027988.2:g.32605del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*81del	ENSP00000513758.1:n.*81del
ENST00000359321.2:c.*81del MANE Select	ENSP00000352271.1:n.*81del
ENST00000359321.1:c.*81del	ENSP00000352271.1:n.*81del
ENST00000495707.1:n.946del
NM_005431.1:c.*81del	NP_005422.1:n.*81del
NM_005431.2:c.*81del MANE Select	NP_005422.1:n.*81del