Canonical Allele Identifier: CA1753247145
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648951C= , CM000669.2:g.152648951C= GRCh38
NC_000007.13:g.152346036C= , CM000669.1:g.152346036C= GRCh37
NC_000007.12:g.151976969C= NCBI36
NG_027988.1:g.32215G=
NG_027988.2:g.32215G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.366G= ENSP00000513758.1:p.Gln122=
ENST00000359321.2:c.534G= MANE Select ENSP00000352271.1:p.Gln178=
ENST00000359321.1:c.534G= ENSP00000352271.1:p.Gln178=
ENST00000495707.1:n.556G=
NM_005431.1:c.534G= NP_005422.1:p.Gln178=
NM_005431.2:c.534G= MANE Select NP_005422.1:p.Gln178=