Canonical Allele Identifier: CA370198023
Gene: XRCC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648735G>C , CM000669.2:g.152648735G>C GRCh38
NC_000007.13:g.152345820G>C , CM000669.1:g.152345820G>C GRCh37
NC_000007.12:g.151976753G>C NCBI36
NG_027988.1:g.32431C>G
NG_027988.2:g.32431C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.582C>G ENSP00000513758.1:p.Ser194Arg
ENST00000359321.2:c.750C>G MANE Select ENSP00000352271.1:p.Ser250Arg
ENST00000359321.1:c.750C>G ENSP00000352271.1:p.Ser250Arg
ENST00000495707.1:n.772C>G
NM_005431.1:c.750C>G NP_005422.1:p.Ser250Arg
NM_005431.2:c.750C>G MANE Select NP_005422.1:p.Ser250Arg