Canonical Allele Identifier: CA1753257174
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660705C= , CM000669.2:g.152660705C= GRCh38
NC_000007.13:g.152357790C= , CM000669.1:g.152357790C= GRCh37
NC_000007.12:g.151988723C= NCBI36
NG_027988.1:g.20461G=
NG_027988.2:g.20461G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11342G= ENSP00000513758.1:n.-47-11342G=
ENST00000698507.1:n.185G=
ENST00000359321.2:c.117G= MANE Select ENSP00000352271.1:p.Val39=
ENST00000359321.1:c.117G= ENSP00000352271.1:p.Val39=
ENST00000495707.1:n.139G=
NM_005431.1:c.117G= NP_005422.1:p.Val39=
NM_005431.2:c.117G= MANE Select NP_005422.1:p.Val39=