Canonical Allele Identifier: CA2778475883
Gene: XRCC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676004T>G , CM000669.2:g.152676004T>G GRCh38
NC_000007.13:g.152373089T>G , CM000669.1:g.152373089T>G GRCh37
NC_000007.12:g.152004022T>G NCBI36
NG_027988.1:g.5162A>C
NG_027988.2:g.5162A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-48+37A>C ENSP00000513758.1:n.-48+37A>C
ENST00000698507.1:n.107+37A>C
ENST00000359321.2:c.39+37A>C MANE Select ENSP00000352271.1:n.39+37A>C
ENST00000359321.1:c.39+37A>C ENSP00000352271.1:n.39+37A>C
NM_005431.1:c.39+37A>C NP_005422.1:n.39+37A>C
NM_005431.2:c.39+37A>C MANE Select NP_005422.1:n.39+37A>C