Canonical Allele Identifier: CA370198057
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152345835A>T (hg19) chr7:g.152648750A>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.567T>A ENSP00000513758.1:p.Asp189Glu
ENST00000359321.2:c.735T>A MANE Select ENSP00000352271.1:p.Asp245Glu
ENST00000359321.1:c.735T>A ENSP00000352271.1:p.Asp245Glu
ENST00000495707.1:n.757T>A
NM_005431.1:c.735T>A NP_005422.1:p.Asp245Glu
NM_005431.2:c.735T>A MANE Select NP_005422.1:p.Asp245Glu
Search 100 bp 5'
Search 100 bp 3'