Canonical Allele Identifier: CA370199453
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660730A>T , CM000669.2:g.152660730A>T GRCh38
NC_000007.13:g.152357815A>T , CM000669.1:g.152357815A>T GRCh37
NC_000007.12:g.151988748A>T NCBI36
NG_027988.1:g.20436T>A
NG_027988.2:g.20436T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11367T>A ENSP00000513758.1:n.-47-11367T>A
ENST00000698507.1:n.160T>A
ENST00000359321.2:c.92T>A MANE Select ENSP00000352271.1:p.Leu31Gln
ENST00000359321.1:c.92T>A ENSP00000352271.1:p.Leu31Gln
ENST00000495707.1:n.114T>A
NM_005431.1:c.92T>A NP_005422.1:p.Leu31Gln
NM_005431.2:c.92T>A MANE Select NP_005422.1:p.Leu31Gln