Canonical Allele Identifier: CA370198719
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.260T>A ENSP00000513758.1:p.Leu87His
ENST00000359321.2:c.428T>A MANE Select ENSP00000352271.1:p.Leu143His
ENST00000359321.1:c.428T>A ENSP00000352271.1:p.Leu143His
ENST00000495707.1:n.450T>A
NM_005431.1:c.428T>A NP_005422.1:p.Leu143His
NM_005431.2:c.428T>A MANE Select NP_005422.1:p.Leu143His