Canonical Allele Identifier: CA2685735609

Gene: XRCC2

Linked Data

• gnomAD v4: 7-152648475-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152648475C>A , CM000669.2:g.152648475C>A	GRCh38
NC_000007.13:g.152345560C>A , CM000669.1:g.152345560C>A	GRCh37
NC_000007.12:g.151976493C>A	NCBI36
NG_027988.1:g.32691G>T
NG_027988.2:g.32691G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.*167G>T	ENSP00000513758.1:n.*167G>T
ENST00000359321.2:c.*167G>T MANE Select	ENSP00000352271.1:n.*167G>T
ENST00000359321.1:c.*167G>T	ENSP00000352271.1:n.*167G>T
ENST00000495707.1:n.1032G>T
NM_005431.1:c.*167G>T	NP_005422.1:n.*167G>T
NM_005431.2:c.*167G>T MANE Select	NP_005422.1:n.*167G>T