Canonical Allele Identifier: CA458895612
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs2116988103
MyVariant Identifiers: chr7:g.152346240G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152649155G>A , CM000669.2:g.152649155G>A GRCh38
NC_000007.13:g.152346240G>A , CM000669.1:g.152346240G>A GRCh37
NC_000007.12:g.151977173G>A NCBI36
NG_027988.1:g.32011C>T
NG_027988.2:g.32011C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000698506.1:c.162C>T ENSP00000513758.1:p.Tyr54=
ENST00000359321.2:c.330C>T MANE Select ENSP00000352271.1:p.Tyr110=
ENST00000359321.1:c.330C>T ENSP00000352271.1:p.Tyr110=
ENST00000495707.1:n.352C>T
NM_005431.1:c.330C>T NP_005422.1:p.Tyr110=
NM_005431.2:c.330C>T MANE Select NP_005422.1:p.Tyr110=