Canonical Allele Identifier: CA370198996
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649180T>C , CM000669.2:g.152649180T>C GRCh38
NC_000007.13:g.152346265T>C , CM000669.1:g.152346265T>C GRCh37
NC_000007.12:g.151977198T>C NCBI36
NG_027988.1:g.31986A>G
NG_027988.2:g.31986A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.137A>G ENSP00000513758.1:p.Gln46Arg
ENST00000359321.2:c.305A>G MANE Select ENSP00000352271.1:p.Gln102Arg
ENST00000359321.1:c.305A>G ENSP00000352271.1:p.Gln102Arg
ENST00000495707.1:n.327A>G
NM_005431.1:c.305A>G NP_005422.1:p.Gln102Arg
NM_005431.2:c.305A>G MANE Select NP_005422.1:p.Gln102Arg