Canonical Allele Identifier: CA1108857354
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648406T>A , CM000669.2:g.152648406T>A GRCh38
NC_000007.13:g.152345491T>A , CM000669.1:g.152345491T>A GRCh37
NC_000007.12:g.151976424T>A NCBI36
NG_027988.1:g.32760A>T
NG_027988.2:g.32760A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*236A>T ENSP00000513758.1:n.*236A>T
ENST00000359321.2:c.*236A>T MANE Select ENSP00000352271.1:n.*236A>T
ENST00000359321.1:c.*236A>T ENSP00000352271.1:n.*236A>T
ENST00000495707.1:n.1101A>T
NM_005431.1:c.*236A>T NP_005422.1:n.*236A>T
NM_005431.2:c.*236A>T MANE Select NP_005422.1:n.*236A>T