Canonical Allele Identifier: CA370198067
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648755G>T , CM000669.2:g.152648755G>T GRCh38
NC_000007.13:g.152345840G>T , CM000669.1:g.152345840G>T GRCh37
NC_000007.12:g.151976773G>T NCBI36
NG_027988.1:g.32411C>A
NG_027988.2:g.32411C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.562C>A ENSP00000513758.1:p.Gln188Lys
ENST00000359321.2:c.730C>A MANE Select ENSP00000352271.1:p.Gln244Lys
ENST00000359321.1:c.730C>A ENSP00000352271.1:p.Gln244Lys
ENST00000495707.1:n.752C>A
NM_005431.1:c.730C>A NP_005422.1:p.Gln244Lys
NM_005431.2:c.730C>A MANE Select NP_005422.1:p.Gln244Lys