Canonical Allele Identifier: CA370198279

Gene: XRCC2

Linked Data

• dbSNP Id: rs1753592953
• MyVariant Identifiers: chr7:g.152345938T>A (hg19) ; chr7:g.152648853T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648853T>A , CM000669.2:g.152648853T>A	GRCh38
NC_000007.13:g.152345938T>A , CM000669.1:g.152345938T>A	GRCh37
NC_000007.12:g.151976871T>A	NCBI36
NG_027988.1:g.32313A>T
NG_027988.2:g.32313A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000698506.1:c.464A>T	ENSP00000513758.1:p.His155Leu
ENST00000359321.2:c.632A>T MANE Select	ENSP00000352271.1:p.His211Leu
ENST00000359321.1:c.632A>T	ENSP00000352271.1:p.His211Leu
ENST00000495707.1:n.654A>T
NM_005431.1:c.632A>T	NP_005422.1:p.His211Leu
NM_005431.2:c.632A>T MANE Select	NP_005422.1:p.His211Leu