Canonical Allele Identifier: CA370199598

Gene: XRCC2

Linked Data

• MyVariant Identifiers: chr7:g.152373140C>A (hg19) ; chr7:g.152676055C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152676055C>A , CM000669.2:g.152676055C>A	GRCh38
NC_000007.13:g.152373140C>A , CM000669.1:g.152373140C>A	GRCh37
NC_000007.12:g.152004073C>A	NCBI36
NG_027988.1:g.5111G>T
NG_027988.2:g.5111G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-62G>T	ENSP00000513758.1:n.-62G>T
ENST00000698507.1:n.93G>T
ENST00000359321.2:c.25G>T MANE Select	ENSP00000352271.1:p.Glu9Ter
ENST00000359321.1:c.25G>T	ENSP00000352271.1:p.Glu9Ter
NM_005431.1:c.25G>T	NP_005422.1:p.Glu9Ter
NM_005431.2:c.25G>T MANE Select	NP_005422.1:p.Glu9Ter