Canonical Allele Identifier: CA835376806
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1196091761
gnomAD v3: 7-152648565-GAC-G
gnomAD v4: 7-152648565-GAC-G
MyVariant Identifiers: chr7:g.152345651_152345652del (hg19) chr7:g.152648566_152648567del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648567_152648568del , CM000669.2:g.152648567_152648568del GRCh38
NC_000007.13:g.152345652_152345653del , CM000669.1:g.152345652_152345653del GRCh37
NC_000007.12:g.151976585_151976586del NCBI36
NG_027988.1:g.32599_32600del
NG_027988.2:g.32599_32600del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*75_*76del ENSP00000513758.1:n.*75_*76del
ENST00000359321.2:c.*75_*76del MANE Select ENSP00000352271.1:n.*75_*76del
ENST00000359321.1:c.*75_*76del ENSP00000352271.1:n.*75_*76del
ENST00000495707.1:n.940_941del
NM_005431.1:c.*75_*76del NP_005422.1:n.*75_*76del
NM_005431.2:c.*75_*76del MANE Select NP_005422.1:n.*75_*76del
Search 100 bp 5'
Search 100 bp 3'