Canonical Allele Identifier: CA2685736362

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152660692-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660692A>C , CM000669.2:g.152660692A>C	GRCh38
NC_000007.13:g.152357777A>C , CM000669.1:g.152357777A>C	GRCh37
NC_000007.12:g.151988710A>C	NCBI36
NG_027988.1:g.20474T>G
NG_027988.2:g.20474T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.-47-11329T>G	ENSP00000513758.1:n.-47-11329T>G
ENST00000698507.1:n.198T>G
ENST00000359321.2:c.121+9T>G MANE Select	ENSP00000352271.1:n.121+9T>G
ENST00000359321.1:c.121+9T>G	ENSP00000352271.1:n.121+9T>G
ENST00000495707.1:n.143+9T>G
NM_005431.1:c.121+9T>G	NP_005422.1:n.121+9T>G
NM_005431.2:c.121+9T>G MANE Select	NP_005422.1:n.121+9T>G