Canonical Allele Identifier: CA370198076

Gene: XRCC2

Linked Data

• dbSNP Id: rs2098027157
• MyVariant Identifiers: chr7:g.152345845G>T (hg19) ; chr7:g.152648760G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648760G>T , CM000669.2:g.152648760G>T	GRCh38
NC_000007.13:g.152345845G>T , CM000669.1:g.152345845G>T	GRCh37
NC_000007.12:g.151976778G>T	NCBI36
NG_027988.1:g.32406C>A
NG_027988.2:g.32406C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.557C>A	ENSP00000513758.1:p.Ser186Tyr
ENST00000359321.2:c.725C>A MANE Select	ENSP00000352271.1:p.Ser242Tyr
ENST00000359321.1:c.725C>A	ENSP00000352271.1:p.Ser242Tyr
ENST00000495707.1:n.747C>A
NM_005431.1:c.725C>A	NP_005422.1:p.Ser242Tyr
NM_005431.2:c.725C>A MANE Select	NP_005422.1:p.Ser242Tyr