Canonical Allele Identifier: CA1753246657
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648741T= , CM000669.2:g.152648741T= GRCh38
NC_000007.13:g.152345826T= , CM000669.1:g.152345826T= GRCh37
NC_000007.12:g.151976759T= NCBI36
NG_027988.1:g.32425A=
NG_027988.2:g.32425A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.576A= ENSP00000513758.1:p.Gln192=
ENST00000359321.2:c.744A= MANE Select ENSP00000352271.1:p.Gln248=
ENST00000359321.1:c.744A= ENSP00000352271.1:p.Gln248=
ENST00000495707.1:n.766A=
NM_005431.1:c.744A= NP_005422.1:p.Gln248=
NM_005431.2:c.744A= MANE Select NP_005422.1:p.Gln248=