Canonical Allele Identifier: CA1753246651
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648738G= , CM000669.2:g.152648738G= GRCh38
NC_000007.13:g.152345823G= , CM000669.1:g.152345823G= GRCh37
NC_000007.12:g.151976756G= NCBI36
NG_027988.1:g.32428C=
NG_027988.2:g.32428C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.579C= ENSP00000513758.1:p.Ser193=
ENST00000359321.2:c.747C= MANE Select ENSP00000352271.1:p.Ser249=
ENST00000359321.1:c.747C= ENSP00000352271.1:p.Ser249=
ENST00000495707.1:n.769C=
NM_005431.1:c.747C= NP_005422.1:p.Ser249=
NM_005431.2:c.747C= MANE Select NP_005422.1:p.Ser249=