Canonical Allele Identifier: CA1753246712
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648760G= , CM000669.2:g.152648760G= GRCh38
NC_000007.13:g.152345845G= , CM000669.1:g.152345845G= GRCh37
NC_000007.12:g.151976778G= NCBI36
NG_027988.1:g.32406C=
NG_027988.2:g.32406C=

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.557C= ENSP00000513758.1:p.Ser186=
ENST00000359321.2:c.725C= MANE Select ENSP00000352271.1:p.Ser242=
ENST00000359321.1:c.725C= ENSP00000352271.1:p.Ser242=
ENST00000495707.1:n.747C=
NM_005431.1:c.725C= NP_005422.1:p.Ser242=
NM_005431.2:c.725C= MANE Select NP_005422.1:p.Ser242=