Canonical Allele Identifier: CA1753257011
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660588T= , CM000669.2:g.152660588T= GRCh38
NC_000007.13:g.152357673T= , CM000669.1:g.152357673T= GRCh37
NC_000007.12:g.151988606T= NCBI36
NG_027988.1:g.20578A=
NG_027988.2:g.20578A=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11225A= ENSP00000513758.1:n.-47-11225A=
ENST00000698507.1:n.302A=
ENST00000359321.2:c.121+113A= MANE Select ENSP00000352271.1:n.121+113A=
ENST00000359321.1:c.121+113A= ENSP00000352271.1:n.121+113A=
ENST00000495707.1:n.143+113A=
NM_005431.1:c.121+113A= NP_005422.1:n.121+113A=
NM_005431.2:c.121+113A= MANE Select NP_005422.1:n.121+113A=