Canonical Allele Identifier: CA322555660
Gene:

Linked Data

ClinVar Variation Id: 1246977
ClinVar RCV Id: RCV001656323
dbSNP Id: rs67279093
gnomAD v2: 22-23915256-AC-A
gnomAD v3: 22-23573069-AC-A
gnomAD v4: 22-23573069-AC-A
MyVariant Identifiers: chr22:g.23915257del (hg19) chr22:g.23573070del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.23573072del , CM000684.2:g.23573072del GRCh38
NC_000022.10:g.23915259del , CM000684.1:g.23915259del GRCh37
NC_000022.9:g.22245259del NCBI36
NG_009791.1:g.12239del , LRG_69:g.12239del

Transcript Alleles

HGVS Amino-acid Change
XR_938075.1:n.713del
XR_938076.1:n.778del
XR_938078.1:n.677del
XR_938079.1:n.570del
XR_938075.2:n.1297del
XR_938078.2:n.1261del
Search 100 bp 5'
Search 100 bp 3'