Canonical Allele Identifier: CA1753246617
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648731G= , CM000669.2:g.152648731G= GRCh38
NC_000007.13:g.152345816G= , CM000669.1:g.152345816G= GRCh37
NC_000007.12:g.151976749G= NCBI36
NG_027988.1:g.32435C=
NG_027988.2:g.32435C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.586C= ENSP00000513758.1:p.Gln196=
ENST00000359321.2:c.754C= MANE Select ENSP00000352271.1:p.Gln252=
ENST00000359321.1:c.754C= ENSP00000352271.1:p.Gln252=
ENST00000495707.1:n.776C=
NM_005431.1:c.754C= NP_005422.1:p.Gln252=
NM_005431.2:c.754C= MANE Select NP_005422.1:p.Gln252=