Canonical Allele Identifier: CA370199459
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660733T>A , CM000669.2:g.152660733T>A GRCh38
NC_000007.13:g.152357818T>A , CM000669.1:g.152357818T>A GRCh37
NC_000007.12:g.151988751T>A NCBI36
NG_027988.1:g.20433A>T
NG_027988.2:g.20433A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11370A>T ENSP00000513758.1:n.-47-11370A>T
ENST00000698507.1:n.157A>T
ENST00000359321.2:c.89A>T MANE Select ENSP00000352271.1:p.Asn30Ile
ENST00000359321.1:c.89A>T ENSP00000352271.1:p.Asn30Ile
ENST00000495707.1:n.111A>T
NM_005431.1:c.89A>T NP_005422.1:p.Asn30Ile
NM_005431.2:c.89A>T MANE Select NP_005422.1:p.Asn30Ile