Canonical Allele Identifier: CA370198066
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1064795954

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.562C>G ENSP00000513758.1:p.Gln188Glu
ENST00000359321.2:c.730C>G MANE Select ENSP00000352271.1:p.Gln244Glu
ENST00000359321.1:c.730C>G ENSP00000352271.1:p.Gln244Glu
ENST00000495707.1:n.752C>G
NM_005431.1:c.730C>G NP_005422.1:p.Gln244Glu
NM_005431.2:c.730C>G MANE Select NP_005422.1:p.Gln244Glu