Canonical Allele Identifier: CA370199584

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152373133C>T (hg19) ; chr7:g.152676048C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676048C>T , CM000669.2:g.152676048C>T	GRCh38
NC_000007.13:g.152373133C>T , CM000669.1:g.152373133C>T	GRCh37
NC_000007.12:g.152004066C>T	NCBI36
NG_027988.1:g.5118G>A
NG_027988.2:g.5118G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-55G>A	ENSP00000513758.1:n.-55G>A
ENST00000698507.1:n.100G>A
ENST00000359321.2:c.32G>A MANE Select	ENSP00000352271.1:p.Gly11Glu
ENST00000359321.1:c.32G>A	ENSP00000352271.1:p.Gly11Glu
NM_005431.1:c.32G>A	NP_005422.1:p.Gly11Glu
NM_005431.2:c.32G>A MANE Select	NP_005422.1:p.Gly11Glu