Canonical Allele Identifier: CA370199476
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660740C>G , CM000669.2:g.152660740C>G GRCh38
NC_000007.13:g.152357825C>G , CM000669.1:g.152357825C>G GRCh37
NC_000007.12:g.151988758C>G NCBI36
NG_027988.1:g.20426G>C
NG_027988.2:g.20426G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.-47-11377G>C ENSP00000513758.1:n.-47-11377G>C
ENST00000698507.1:n.150G>C
ENST00000359321.2:c.82G>C MANE Select ENSP00000352271.1:p.Glu28Gln
ENST00000359321.1:c.82G>C ENSP00000352271.1:p.Glu28Gln
ENST00000495707.1:n.104G>C
NM_005431.1:c.82G>C NP_005422.1:p.Glu28Gln
NM_005431.2:c.82G>C MANE Select NP_005422.1:p.Glu28Gln