Canonical Allele Identifier: CA370199540

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152357854A>T (hg19) ; chr7:g.152660769A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660769A>T , CM000669.2:g.152660769A>T	GRCh38
NC_000007.13:g.152357854A>T , CM000669.1:g.152357854A>T	GRCh37
NC_000007.12:g.151988787A>T	NCBI36
NG_027988.1:g.20397T>A
NG_027988.2:g.20397T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-47-11406T>A	ENSP00000513758.1:n.-47-11406T>A
ENST00000698507.1:n.121T>A
ENST00000359321.2:c.53T>A MANE Select	ENSP00000352271.1:p.Leu18His
ENST00000359321.1:c.53T>A	ENSP00000352271.1:p.Leu18His
ENST00000495707.1:n.75T>A
NM_005431.1:c.53T>A	NP_005422.1:p.Leu18His
NM_005431.2:c.53T>A MANE Select	NP_005422.1:p.Leu18His