Canonical Allele Identifier: CA370199591
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152373137A>G (hg19) chr7:g.152676052A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152676052A>G , CM000669.2:g.152676052A>G GRCh38
NC_000007.13:g.152373137A>G , CM000669.1:g.152373137A>G GRCh37
NC_000007.12:g.152004070A>G NCBI36
NG_027988.1:g.5114T>C
NG_027988.2:g.5114T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.-59T>C ENSP00000513758.1:n.-59T>C
ENST00000698507.1:n.96T>C
ENST00000359321.2:c.28T>C MANE Select ENSP00000352271.1:p.Ser10Pro
ENST00000359321.1:c.28T>C ENSP00000352271.1:p.Ser10Pro
NM_005431.1:c.28T>C NP_005422.1:p.Ser10Pro
NM_005431.2:c.28T>C MANE Select NP_005422.1:p.Ser10Pro
Search 100 bp 5'
Search 100 bp 3'