Canonical Allele Identifier: CA4582406
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs772509446

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660739T>C , CM000669.2:g.152660739T>C GRCh38
NC_000007.13:g.152357824T>C , CM000669.1:g.152357824T>C GRCh37
NC_000007.12:g.151988757T>C NCBI36
NG_027988.1:g.20427A>G
NG_027988.2:g.20427A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11376A>G ENSP00000513758.1:n.-47-11376A>G
ENST00000698507.1:n.151A>G
ENST00000359321.2:c.83A>G MANE Select ENSP00000352271.1:p.Glu28Gly
ENST00000359321.1:c.83A>G ENSP00000352271.1:p.Glu28Gly
ENST00000495707.1:n.105A>G
NM_005431.1:c.83A>G NP_005422.1:p.Glu28Gly
NM_005431.2:c.83A>G MANE Select NP_005422.1:p.Glu28Gly