Canonical Allele Identifier: CA458895300

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152346039A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648954A>G , CM000669.2:g.152648954A>G	GRCh38
NC_000007.13:g.152346039A>G , CM000669.1:g.152346039A>G	GRCh37
NC_000007.12:g.151976972A>G	NCBI36
NG_027988.1:g.32212T>C
NG_027988.2:g.32212T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.363T>C	ENSP00000513758.1:p.Ser121=
ENST00000359321.2:c.531T>C MANE Select	ENSP00000352271.1:p.Ser177=
ENST00000359321.1:c.531T>C	ENSP00000352271.1:p.Ser177=
ENST00000495707.1:n.553T>C
NM_005431.1:c.531T>C	NP_005422.1:p.Ser177=
NM_005431.2:c.531T>C MANE Select	NP_005422.1:p.Ser177=