Canonical Allele Identifier: CA1753274857
Gene: XRCC2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676109C= , CM000669.2:g.152676109C= GRCh38
NC_000007.13:g.152373194C= , CM000669.1:g.152373194C= GRCh37
NC_000007.12:g.152004127C= NCBI36
NG_027988.1:g.5057G=
NG_027988.2:g.5057G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-116G= ENSP00000513758.1:n.-116G=
ENST00000698507.1:n.39G=
ENST00000359321.2:c.-30G= MANE Select ENSP00000352271.1:n.-30G=
ENST00000359321.1:c.-30G= ENSP00000352271.1:n.-30G=
NM_005431.1:c.-30G= NP_005422.1:n.-30G=
NM_005431.2:c.-30G= MANE Select NP_005422.1:n.-30G=
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