Canonical Allele Identifier: CA458895447
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2116987578
MyVariant Identifiers: chr7:g.152346015A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648930A>G , CM000669.2:g.152648930A>G GRCh38
NC_000007.13:g.152346015A>G , CM000669.1:g.152346015A>G GRCh37
NC_000007.12:g.151976948A>G NCBI36
NG_027988.1:g.32236T>C
NG_027988.2:g.32236T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.387T>C ENSP00000513758.1:p.Asn129=
ENST00000359321.2:c.555T>C MANE Select ENSP00000352271.1:p.Asn185=
ENST00000359321.1:c.555T>C ENSP00000352271.1:p.Asn185=
ENST00000495707.1:n.577T>C
NM_005431.1:c.555T>C NP_005422.1:p.Asn185=
NM_005431.2:c.555T>C MANE Select NP_005422.1:p.Asn185=