Canonical Allele Identifier: CA370198455
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648938G>A , CM000669.2:g.152648938G>A GRCh38
NC_000007.13:g.152346023G>A , CM000669.1:g.152346023G>A GRCh37
NC_000007.12:g.151976956G>A NCBI36
NG_027988.1:g.32228C>T
NG_027988.2:g.32228C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.379C>T ENSP00000513758.1:p.Leu127Phe
ENST00000359321.2:c.547C>T MANE Select ENSP00000352271.1:p.Leu183Phe
ENST00000359321.1:c.547C>T ENSP00000352271.1:p.Leu183Phe
ENST00000495707.1:n.569C>T
NM_005431.1:c.547C>T NP_005422.1:p.Leu183Phe
NM_005431.2:c.547C>T MANE Select NP_005422.1:p.Leu183Phe