Canonical Allele Identifier: CA1753274603
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676043C= , CM000669.2:g.152676043C= GRCh38
NC_000007.13:g.152373128C= , CM000669.1:g.152373128C= GRCh37
NC_000007.12:g.152004061C= NCBI36
NG_027988.1:g.5123G=
NG_027988.2:g.5123G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-50G= ENSP00000513758.1:n.-50G=
ENST00000698507.1:n.105G=
ENST00000359321.2:c.37G= MANE Select ENSP00000352271.1:p.Glu13=
ENST00000359321.1:c.37G= ENSP00000352271.1:p.Glu13=
NM_005431.1:c.37G= NP_005422.1:p.Glu13=
NM_005431.2:c.37G= MANE Select NP_005422.1:p.Glu13=