Canonical Allele Identifier: CA2716215889

Gene: XRCC2

Linked Data

• dbSNP Id: rs2117014279

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152675980del , CM000669.2:g.152675980del	GRCh38
NC_000007.13:g.152373065del , CM000669.1:g.152373065del	GRCh37
NC_000007.12:g.152003998del	NCBI36
NG_027988.1:g.5186del
NG_027988.2:g.5186del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48+61del	ENSP00000513758.1:n.-48+61del
ENST00000698507.1:n.107+61del
ENST00000359321.2:c.39+61del MANE Select	ENSP00000352271.1:n.39+61del
ENST00000359321.1:c.39+61del	ENSP00000352271.1:n.39+61del
NM_005431.1:c.39+61del	NP_005422.1:n.39+61del
NM_005431.2:c.39+61del MANE Select	NP_005422.1:n.39+61del