Canonical Allele Identifier: CA370199486
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152357830T>G (hg19) chr7:g.152660745T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152660745T>G , CM000669.2:g.152660745T>G GRCh38
NC_000007.13:g.152357830T>G , CM000669.1:g.152357830T>G GRCh37
NC_000007.12:g.151988763T>G NCBI36
NG_027988.1:g.20421A>C
NG_027988.2:g.20421A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-47-11382A>C ENSP00000513758.1:n.-47-11382A>C
ENST00000698507.1:n.145A>C
ENST00000359321.2:c.77A>C MANE Select ENSP00000352271.1:p.Glu26Ala
ENST00000359321.1:c.77A>C ENSP00000352271.1:p.Glu26Ala
ENST00000495707.1:n.99A>C
NM_005431.1:c.77A>C NP_005422.1:p.Glu26Ala
NM_005431.2:c.77A>C MANE Select NP_005422.1:p.Glu26Ala
Search 100 bp 5'
Search 100 bp 3'