Canonical Allele Identifier: CA835376680
Gene: XRCC2 HGNC NCBI

Linked Data

dbSNP Id: rs1277640841
gnomAD v3: 7-152648407-CAAAAAGAAAAAAAAAA-C
gnomAD v4: 7-152648407-CAAAAAGAAAAAAAAAA-C
MyVariant Identifiers: chr7:g.152345493_152345508del (hg19) chr7:g.152648408_152648423del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.152648418_152648433del , CM000669.2:g.152648418_152648433del GRCh38
NC_000007.13:g.152345503_152345518del , CM000669.1:g.152345503_152345518del GRCh37
NC_000007.12:g.151976436_151976451del NCBI36
NG_027988.1:g.32743_32758del
NG_027988.2:g.32743_32758del

Transcript Alleles

HGVS Amino-acid Change
ENST00000698506.1:c.*219_*234del ENSP00000513758.1:n.*219_*234del
ENST00000359321.2:c.*219_*234del MANE Select ENSP00000352271.1:n.*219_*234del
ENST00000359321.1:c.*219_*234del ENSP00000352271.1:n.*219_*234del
ENST00000495707.1:n.1084_1099del
NM_005431.1:c.*219_*234del NP_005422.1:n.*219_*234del
NM_005431.2:c.*219_*234del MANE Select NP_005422.1:n.*219_*234del
Search 100 bp 5'
Search 100 bp 3'