Canonical Allele Identifier: CA370199572
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676042T>G , CM000669.2:g.152676042T>G GRCh38
NC_000007.13:g.152373127T>G , CM000669.1:g.152373127T>G GRCh37
NC_000007.12:g.152004060T>G NCBI36
NG_027988.1:g.5124A>C
NG_027988.2:g.5124A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-49A>C ENSP00000513758.1:n.-49A>C
ENST00000698507.1:n.106A>C
ENST00000359321.2:c.38A>C MANE Select ENSP00000352271.1:p.Glu13Ala
ENST00000359321.1:c.38A>C ENSP00000352271.1:p.Glu13Ala
NM_005431.1:c.38A>C NP_005422.1:p.Glu13Ala
NM_005431.2:c.38A>C MANE Select NP_005422.1:p.Glu13Ala