Canonical Allele Identifier: CA370198155

Gene: XRCC2

Linked Data

• dbSNP Id: rs1267462913
• MyVariant Identifiers: chr7:g.152345877C>T (hg19) ; chr7:g.152648792C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648792C>T , CM000669.2:g.152648792C>T	GRCh38
NC_000007.13:g.152345877C>T , CM000669.1:g.152345877C>T	GRCh37
NC_000007.12:g.151976810C>T	NCBI36
NG_027988.1:g.32374G>A
NG_027988.2:g.32374G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.525G>A	ENSP00000513758.1:p.Trp175Ter
ENST00000359321.2:c.693G>A MANE Select	ENSP00000352271.1:p.Trp231Ter
ENST00000359321.1:c.693G>A	ENSP00000352271.1:p.Trp231Ter
ENST00000495707.1:n.715G>A
NM_005431.1:c.693G>A	NP_005422.1:p.Trp231Ter
NM_005431.2:c.693G>A MANE Select	NP_005422.1:p.Trp231Ter