Canonical Allele Identifier: CA370198268
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152345932G>T (hg19) chr7:g.152648847G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648847G>T , CM000669.2:g.152648847G>T GRCh38
NC_000007.13:g.152345932G>T , CM000669.1:g.152345932G>T GRCh37
NC_000007.12:g.151976865G>T NCBI36
NG_027988.1:g.32319C>A
NG_027988.2:g.32319C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.470C>A ENSP00000513758.1:p.Ser157Tyr
ENST00000359321.2:c.638C>A MANE Select ENSP00000352271.1:p.Ser213Tyr
ENST00000359321.1:c.638C>A ENSP00000352271.1:p.Ser213Tyr
ENST00000495707.1:n.660C>A
NM_005431.1:c.638C>A NP_005422.1:p.Ser213Tyr
NM_005431.2:c.638C>A MANE Select NP_005422.1:p.Ser213Tyr
Search 100 bp 5'
Search 100 bp 3'