Canonical Allele Identifier: CA370198718
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649057A>G , CM000669.2:g.152649057A>G GRCh38
NC_000007.13:g.152346142A>G , CM000669.1:g.152346142A>G GRCh37
NC_000007.12:g.151977075A>G NCBI36
NG_027988.1:g.32109T>C
NG_027988.2:g.32109T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.260T>C ENSP00000513758.1:p.Leu87Pro
ENST00000359321.2:c.428T>C MANE Select ENSP00000352271.1:p.Leu143Pro
ENST00000359321.1:c.428T>C ENSP00000352271.1:p.Leu143Pro
ENST00000495707.1:n.450T>C
NM_005431.1:c.428T>C NP_005422.1:p.Leu143Pro
NM_005431.2:c.428T>C MANE Select NP_005422.1:p.Leu143Pro