Canonical Allele Identifier: CA370197875

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152648670-A-G
• MyVariant Identifiers: chr7:g.152345755A>G (hg19) ; chr7:g.152648670A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648670A>G , CM000669.2:g.152648670A>G	GRCh38
NC_000007.13:g.152345755A>G , CM000669.1:g.152345755A>G	GRCh37
NC_000007.12:g.151976688A>G	NCBI36
NG_027988.1:g.32496T>C
NG_027988.2:g.32496T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.647T>C	ENSP00000513758.1:p.Ile216Thr
ENST00000359321.2:c.815T>C MANE Select	ENSP00000352271.1:p.Ile272Thr
ENST00000359321.1:c.815T>C	ENSP00000352271.1:p.Ile272Thr
ENST00000495707.1:n.837T>C
NM_005431.1:c.815T>C	NP_005422.1:p.Ile272Thr
NM_005431.2:c.815T>C MANE Select	NP_005422.1:p.Ile272Thr