Canonical Allele Identifier: CA169486915
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs928108256
gnomAD v3: 7-152648424-AAAAAG-A
gnomAD v4: 7-152648424-AAAAAG-A
MyVariant Identifiers: chr7:g.152345510_152345514del (hg19) chr7:g.152648425_152648429del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648429_152648433del , CM000669.2:g.152648429_152648433del GRCh38
NC_000007.13:g.152345514_152345518del , CM000669.1:g.152345514_152345518del GRCh37
NC_000007.12:g.151976447_151976451del NCBI36
NG_027988.1:g.32737_32741del
NG_027988.2:g.32737_32741del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*213_*217del ENSP00000513758.1:n.*213_*217del
ENST00000359321.2:c.*213_*217del MANE Select ENSP00000352271.1:n.*213_*217del
ENST00000359321.1:c.*213_*217del ENSP00000352271.1:n.*213_*217del
ENST00000495707.1:n.1078_1082del
NM_005431.1:c.*213_*217del NP_005422.1:n.*213_*217del
NM_005431.2:c.*213_*217del MANE Select NP_005422.1:n.*213_*217del
Search 100 bp 5'
Search 100 bp 3'