Canonical Allele Identifier: CA370199462
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660734T>A , CM000669.2:g.152660734T>A GRCh38
NC_000007.13:g.152357819T>A , CM000669.1:g.152357819T>A GRCh37
NC_000007.12:g.151988752T>A NCBI36
NG_027988.1:g.20432A>T
NG_027988.2:g.20432A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11371A>T ENSP00000513758.1:n.-47-11371A>T
ENST00000698507.1:n.156A>T
ENST00000359321.2:c.88A>T MANE Select ENSP00000352271.1:p.Asn30Tyr
ENST00000359321.1:c.88A>T ENSP00000352271.1:p.Asn30Tyr
ENST00000495707.1:n.110A>T
NM_005431.1:c.88A>T NP_005422.1:p.Asn30Tyr
NM_005431.2:c.88A>T MANE Select NP_005422.1:p.Asn30Tyr