Canonical Allele Identifier: CA370199589

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152373136G>T (hg19) ; chr7:g.152676051G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676051G>T , CM000669.2:g.152676051G>T	GRCh38
NC_000007.13:g.152373136G>T , CM000669.1:g.152373136G>T	GRCh37
NC_000007.12:g.152004069G>T	NCBI36
NG_027988.1:g.5115C>A
NG_027988.2:g.5115C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-58C>A	ENSP00000513758.1:n.-58C>A
ENST00000698507.1:n.97C>A
ENST00000359321.2:c.29C>A MANE Select	ENSP00000352271.1:p.Ser10Tyr
ENST00000359321.1:c.29C>A	ENSP00000352271.1:p.Ser10Tyr
NM_005431.1:c.29C>A	NP_005422.1:p.Ser10Tyr
NM_005431.2:c.29C>A MANE Select	NP_005422.1:p.Ser10Tyr