Canonical Allele Identifier: CA811040070
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1388527532
gnomAD v3: 5-44662476-CT-C
gnomAD v4: 5-44662476-CT-C
MyVariant Identifiers: chr5:g.44662579del (hg19) chr5:g.44662477del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662479del , CM000667.2:g.44662479del GRCh38
NC_000005.9:g.44662581del , CM000667.1:g.44662581del GRCh37
NC_000005.8:g.44698338del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3920del
XR_925983.1:n.71-3920del
Search 100 bp 5'
Search 100 bp 3'