Canonical Allele Identifier: CA1753256988
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660544G= , CM000669.2:g.152660544G= GRCh38
NC_000007.13:g.152357629G= , CM000669.1:g.152357629G= GRCh37
NC_000007.12:g.151988562G= NCBI36
NG_027988.1:g.20622C=
NG_027988.2:g.20622C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11181C= ENSP00000513758.1:n.-47-11181C=
ENST00000698507.1:n.346C=
ENST00000359321.2:c.121+157C= MANE Select ENSP00000352271.1:n.121+157C=
ENST00000359321.1:c.121+157C= ENSP00000352271.1:n.121+157C=
ENST00000495707.1:n.143+157C=
NM_005431.1:c.121+157C= NP_005422.1:n.121+157C=
NM_005431.2:c.121+157C= MANE Select NP_005422.1:n.121+157C=