Canonical Allele Identifier: CA458895248
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152345835A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648750A>G , CM000669.2:g.152648750A>G GRCh38
NC_000007.13:g.152345835A>G , CM000669.1:g.152345835A>G GRCh37
NC_000007.12:g.151976768A>G NCBI36
NG_027988.1:g.32416T>C
NG_027988.2:g.32416T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.567T>C ENSP00000513758.1:p.Asp189=
ENST00000359321.2:c.735T>C MANE Select ENSP00000352271.1:p.Asp245=
ENST00000359321.1:c.735T>C ENSP00000352271.1:p.Asp245=
ENST00000495707.1:n.757T>C
NM_005431.1:c.735T>C NP_005422.1:p.Asp245=
NM_005431.2:c.735T>C MANE Select NP_005422.1:p.Asp245=
Search 100 bp 5'
Search 100 bp 3'