Canonical Allele Identifier: CA370199026

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152346279C>G (hg19) ; chr7:g.152649194C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152649194C>G , CM000669.2:g.152649194C>G	GRCh38
NC_000007.13:g.152346279C>G , CM000669.1:g.152346279C>G	GRCh37
NC_000007.12:g.151977212C>G	NCBI36
NG_027988.1:g.31972G>C
NG_027988.2:g.31972G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.123G>C	ENSP00000513758.1:p.Glu41Asp
ENST00000359321.2:c.291G>C MANE Select	ENSP00000352271.1:p.Glu97Asp
ENST00000359321.1:c.291G>C	ENSP00000352271.1:p.Glu97Asp
ENST00000495707.1:n.313G>C
NM_005431.1:c.291G>C	NP_005422.1:p.Glu97Asp
NM_005431.2:c.291G>C MANE Select	NP_005422.1:p.Glu97Asp