Canonical Allele Identifier: CA1753246379
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648486A= , CM000669.2:g.152648486A= GRCh38
NC_000007.13:g.152345571A= , CM000669.1:g.152345571A= GRCh37
NC_000007.12:g.151976504A= NCBI36
NG_027988.1:g.32680T=
NG_027988.2:g.32680T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*156T= ENSP00000513758.1:n.*156T=
ENST00000359321.2:c.*156T= MANE Select ENSP00000352271.1:n.*156T=
ENST00000359321.1:c.*156T= ENSP00000352271.1:n.*156T=
ENST00000495707.1:n.1021T=
NM_005431.1:c.*156T= NP_005422.1:n.*156T=
NM_005431.2:c.*156T= MANE Select NP_005422.1:n.*156T=