Canonical Allele Identifier: CA1753247128
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648939C= , CM000669.2:g.152648939C= GRCh38
NC_000007.13:g.152346024C= , CM000669.1:g.152346024C= GRCh37
NC_000007.12:g.151976957C= NCBI36
NG_027988.1:g.32227G=
NG_027988.2:g.32227G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.378G= ENSP00000513758.1:p.Lys126=
ENST00000359321.2:c.546G= MANE Select ENSP00000352271.1:p.Lys182=
ENST00000359321.1:c.546G= ENSP00000352271.1:p.Lys182=
ENST00000495707.1:n.568G=
NM_005431.1:c.546G= NP_005422.1:p.Lys182=
NM_005431.2:c.546G= MANE Select NP_005422.1:p.Lys182=