Canonical Allele Identifier: CA811039988
Gene: LINC02224 HGNC NCBI

Linked Data

dbSNP Id: rs1390546376
gnomAD v3: 5-44662394-AT-A
gnomAD v4: 5-44662394-AT-A
MyVariant Identifiers: chr5:g.44662497del (hg19) chr5:g.44662395del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.44662396del , CM000667.2:g.44662396del GRCh38
NC_000005.9:g.44662498del , CM000667.1:g.44662498del GRCh37
NC_000005.8:g.44698255del NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_427699.2:n.92-3838del
XR_925983.1:n.71-3838del
Search 100 bp 5'
Search 100 bp 3'