Canonical Allele Identifier: CA1753247569
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649158T= , CM000669.2:g.152649158T= GRCh38
NC_000007.13:g.152346243T= , CM000669.1:g.152346243T= GRCh37
NC_000007.12:g.151977176T= NCBI36
NG_027988.1:g.32008A=
NG_027988.2:g.32008A=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.159A= ENSP00000513758.1:p.Lys53=
ENST00000359321.2:c.327A= MANE Select ENSP00000352271.1:p.Lys109=
ENST00000359321.1:c.327A= ENSP00000352271.1:p.Lys109=
ENST00000495707.1:n.349A=
NM_005431.1:c.327A= NP_005422.1:p.Lys109=
NM_005431.2:c.327A= MANE Select NP_005422.1:p.Lys109=