Canonical Allele Identifier: CA458805212

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152373132C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676047C>G , CM000669.2:g.152676047C>G	GRCh38
NC_000007.13:g.152373132C>G , CM000669.1:g.152373132C>G	GRCh37
NC_000007.12:g.152004065C>G	NCBI36
NG_027988.1:g.5119G>C
NG_027988.2:g.5119G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-54G>C	ENSP00000513758.1:n.-54G>C
ENST00000698507.1:n.101G>C
ENST00000359321.2:c.33G>C MANE Select	ENSP00000352271.1:p.Gly11=
ENST00000359321.1:c.33G>C	ENSP00000352271.1:p.Gly11=
NM_005431.1:c.33G>C	NP_005422.1:p.Gly11=
NM_005431.2:c.33G>C MANE Select	NP_005422.1:p.Gly11=