Canonical Allele Identifier: CA370198222

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152648822-T-C
• MyVariant Identifiers: chr7:g.152345907T>C (hg19) ; chr7:g.152648822T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648822T>C , CM000669.2:g.152648822T>C	GRCh38
NC_000007.13:g.152345907T>C , CM000669.1:g.152345907T>C	GRCh37
NC_000007.12:g.151976840T>C	NCBI36
NG_027988.1:g.32344A>G
NG_027988.2:g.32344A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.495A>G	ENSP00000513758.1:p.Ile165Met
ENST00000359321.2:c.663A>G MANE Select	ENSP00000352271.1:p.Ile221Met
ENST00000359321.1:c.663A>G	ENSP00000352271.1:p.Ile221Met
ENST00000495707.1:n.685A>G
NM_005431.1:c.663A>G	NP_005422.1:p.Ile221Met
NM_005431.2:c.663A>G MANE Select	NP_005422.1:p.Ile221Met