Canonical Allele Identifier: CA458895455

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152346024C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648939C>T , CM000669.2:g.152648939C>T	GRCh38
NC_000007.13:g.152346024C>T , CM000669.1:g.152346024C>T	GRCh37
NC_000007.12:g.151976957C>T	NCBI36
NG_027988.1:g.32227G>A
NG_027988.2:g.32227G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.378G>A	ENSP00000513758.1:p.Lys126=
ENST00000359321.2:c.546G>A MANE Select	ENSP00000352271.1:p.Lys182=
ENST00000359321.1:c.546G>A	ENSP00000352271.1:p.Lys182=
ENST00000495707.1:n.568G>A
NM_005431.1:c.546G>A	NP_005422.1:p.Lys182=
NM_005431.2:c.546G>A MANE Select	NP_005422.1:p.Lys182=