Canonical Allele Identifier: CA370198938
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649156T>G , CM000669.2:g.152649156T>G GRCh38
NC_000007.13:g.152346241T>G , CM000669.1:g.152346241T>G GRCh37
NC_000007.12:g.151977174T>G NCBI36
NG_027988.1:g.32010A>C
NG_027988.2:g.32010A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.161A>C ENSP00000513758.1:p.Tyr54Ser
ENST00000359321.2:c.329A>C MANE Select ENSP00000352271.1:p.Tyr110Ser
ENST00000359321.1:c.329A>C ENSP00000352271.1:p.Tyr110Ser
ENST00000495707.1:n.351A>C
NM_005431.1:c.329A>C NP_005422.1:p.Tyr110Ser
NM_005431.2:c.329A>C MANE Select NP_005422.1:p.Tyr110Ser