Canonical Allele Identifier: CA370198074
Gene: XRCC2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2560334
ClinVar RCV Id: RCV003310007
MyVariant Identifiers: chr7:g.152345843T>C (hg19) chr7:g.152648758T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648758T>C , CM000669.2:g.152648758T>C GRCh38
NC_000007.13:g.152345843T>C , CM000669.1:g.152345843T>C GRCh37
NC_000007.12:g.151976776T>C NCBI36
NG_027988.1:g.32408A>G
NG_027988.2:g.32408A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.559A>G ENSP00000513758.1:p.Lys187Glu
ENST00000359321.2:c.727A>G MANE Select ENSP00000352271.1:p.Lys243Glu
ENST00000359321.1:c.727A>G ENSP00000352271.1:p.Lys243Glu
ENST00000495707.1:n.749A>G
NM_005431.1:c.727A>G NP_005422.1:p.Lys243Glu
NM_005431.2:c.727A>G MANE Select NP_005422.1:p.Lys243Glu
Search 100 bp 5'
Search 100 bp 3'