Canonical Allele Identifier: CA356463

Gene: XRCC2

Linked Data

• ClinVar Variation Id: 224934
• ClinVar RCV Id: RCV000210512 ; RCV000857960 ; RCV003316162
• dbSNP Id: rs3218472
• ExAC: 7:152357877 G / A
• gnomAD v2: 7-152357877-G-A
• gnomAD v3: 7-152660792-G-A
• gnomAD v4: 7-152660792-G-A
• MyVariant Identifiers: chr7:g.152357877G>A (hg19) ; chr7:g.152660792G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.152660792G>A , CM000669.2:g.152660792G>A	GRCh38
NC_000007.13:g.152357877G>A , CM000669.1:g.152357877G>A	GRCh37
NC_000007.12:g.151988810G>A	NCBI36
NG_027988.1:g.20374C>T
NG_027988.2:g.20374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000698506.1:c.-47-11429C>T	ENSP00000513758.1:n.-47-11429C>T
ENST00000698507.1:n.108-10C>T
ENST00000359321.2:c.40-10C>T MANE Select	ENSP00000352271.1:n.40-10C>T
ENST00000359321.1:c.40-10C>T	ENSP00000352271.1:n.40-10C>T
ENST00000495707.1:n.62-10C>T
NM_005431.1:c.40-10C>T	NP_005422.1:n.40-10C>T
NM_005431.2:c.40-10C>T MANE Select	NP_005422.1:n.40-10C>T