Canonical Allele Identifier: CA1108867623

Gene: XRCC2

Linked Data

• dbSNP Id: rs2098040563
• gnomAD v3: 7-152675578-C-CTACA
• gnomAD v4: 7-152675578-C-CTACA

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152675579_152675582dup , CM000669.2:g.152675579_152675582dup	GRCh38
NC_000007.13:g.152372664_152372667dup , CM000669.1:g.152372664_152372667dup	GRCh37
NC_000007.12:g.152003597_152003600dup	NCBI36
NG_027988.1:g.5584_5587dup
NG_027988.2:g.5584_5587dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-48+459_-48+462dup	ENSP00000513758.1:n.-48+459_-48+462dup
ENST00000698507.1:n.107+459_107+462dup
ENST00000359321.2:c.39+459_39+462dup MANE Select	ENSP00000352271.1:n.39+459_39+462dup
ENST00000359321.1:c.39+459_39+462dup	ENSP00000352271.1:n.39+459_39+462dup
NM_005431.1:c.39+459_39+462dup	NP_005422.1:n.39+459_39+462dup
NM_005431.2:c.39+459_39+462dup MANE Select	NP_005422.1:n.39+459_39+462dup