Canonical Allele Identifier: CA458895299
Gene: XRCC2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.152346039A>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648954A>C , CM000669.2:g.152648954A>C GRCh38
NC_000007.13:g.152346039A>C , CM000669.1:g.152346039A>C GRCh37
NC_000007.12:g.151976972A>C NCBI36
NG_027988.1:g.32212T>G
NG_027988.2:g.32212T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.363T>G ENSP00000513758.1:p.Ser121=
ENST00000359321.2:c.531T>G MANE Select ENSP00000352271.1:p.Ser177=
ENST00000359321.1:c.531T>G ENSP00000352271.1:p.Ser177=
ENST00000495707.1:n.553T>G
NM_005431.1:c.531T>G NP_005422.1:p.Ser177=
NM_005431.2:c.531T>G MANE Select NP_005422.1:p.Ser177=
Search 100 bp 5'
Search 100 bp 3'