Canonical Allele Identifier: CA1108867622

Gene: XRCC2

Linked Data

• dbSNP Id: rs2098040560
• gnomAD v3: 7-152675577-G-A
• gnomAD v4: 7-152675577-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152675577G>A , CM000669.2:g.152675577G>A	GRCh38
NC_000007.13:g.152372662G>A , CM000669.1:g.152372662G>A	GRCh37
NC_000007.12:g.152003595G>A	NCBI36
NG_027988.1:g.5589C>T
NG_027988.2:g.5589C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48+464C>T	ENSP00000513758.1:n.-48+464C>T
ENST00000698507.1:n.107+464C>T
ENST00000359321.2:c.39+464C>T MANE Select	ENSP00000352271.1:n.39+464C>T
ENST00000359321.1:c.39+464C>T	ENSP00000352271.1:n.39+464C>T
NM_005431.1:c.39+464C>T	NP_005422.1:n.39+464C>T
NM_005431.2:c.39+464C>T MANE Select	NP_005422.1:n.39+464C>T