Canonical Allele Identifier: CA1753274623
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676049C= , CM000669.2:g.152676049C= GRCh38
NC_000007.13:g.152373134C= , CM000669.1:g.152373134C= GRCh37
NC_000007.12:g.152004067C= NCBI36
NG_027988.1:g.5117G=
NG_027988.2:g.5117G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-56G= ENSP00000513758.1:n.-56G=
ENST00000698507.1:n.99G=
ENST00000359321.2:c.31G= MANE Select ENSP00000352271.1:p.Gly11=
ENST00000359321.1:c.31G= ENSP00000352271.1:p.Gly11=
NM_005431.1:c.31G= NP_005422.1:p.Gly11=
NM_005431.2:c.31G= MANE Select NP_005422.1:p.Gly11=