Canonical Allele Identifier: CA16618435
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1064794116

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649145T>A , CM000669.2:g.152649145T>A GRCh38
NC_000007.13:g.152346230T>A , CM000669.1:g.152346230T>A GRCh37
NC_000007.12:g.151977163T>A NCBI36
NG_027988.1:g.32021A>T
NG_027988.2:g.32021A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.172A>T ENSP00000513758.1:p.Arg58Ter
ENST00000359321.2:c.340A>T MANE Select ENSP00000352271.1:p.Arg114Ter
ENST00000359321.1:c.340A>T ENSP00000352271.1:p.Arg114Ter
ENST00000495707.1:n.362A>T
NM_005431.1:c.340A>T NP_005422.1:p.Arg114Ter
NM_005431.2:c.340A>T MANE Select NP_005422.1:p.Arg114Ter