Canonical Allele Identifier: CA370197959
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648705T>G , CM000669.2:g.152648705T>G GRCh38
NC_000007.13:g.152345790T>G , CM000669.1:g.152345790T>G GRCh37
NC_000007.12:g.151976723T>G NCBI36
NG_027988.1:g.32461A>C
NG_027988.2:g.32461A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.612A>C ENSP00000513758.1:p.Leu204Phe
ENST00000359321.2:c.780A>C MANE Select ENSP00000352271.1:p.Leu260Phe
ENST00000359321.1:c.780A>C ENSP00000352271.1:p.Leu260Phe
ENST00000495707.1:n.802A>C
NM_005431.1:c.780A>C NP_005422.1:p.Leu260Phe
NM_005431.2:c.780A>C MANE Select NP_005422.1:p.Leu260Phe