Canonical Allele Identifier: CA1753274211
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152675763T= , CM000669.2:g.152675763T= GRCh38
NC_000007.13:g.152372848T= , CM000669.1:g.152372848T= GRCh37
NC_000007.12:g.152003781T= NCBI36
NG_027988.1:g.5403A=
NG_027988.2:g.5403A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+278A= ENSP00000513758.1:n.-48+278A=
ENST00000698507.1:n.107+278A=
ENST00000359321.2:c.39+278A= MANE Select ENSP00000352271.1:n.39+278A=
ENST00000359321.1:c.39+278A= ENSP00000352271.1:n.39+278A=
NM_005431.1:c.39+278A= NP_005422.1:n.39+278A=
NM_005431.2:c.39+278A= MANE Select NP_005422.1:n.39+278A=