Canonical Allele Identifier: CA370198983
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649175A>T , CM000669.2:g.152649175A>T GRCh38
NC_000007.13:g.152346260A>T , CM000669.1:g.152346260A>T GRCh37
NC_000007.12:g.151977193A>T NCBI36
NG_027988.1:g.31991T>A
NG_027988.2:g.31991T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.142T>A ENSP00000513758.1:p.Ser48Thr
ENST00000359321.2:c.310T>A MANE Select ENSP00000352271.1:p.Ser104Thr
ENST00000359321.1:c.310T>A ENSP00000352271.1:p.Ser104Thr
ENST00000495707.1:n.332T>A
NM_005431.1:c.310T>A NP_005422.1:p.Ser104Thr
NM_005431.2:c.310T>A MANE Select NP_005422.1:p.Ser104Thr