Canonical Allele Identifier: CA703248171
Gene: LINC02323 HGNC NCBI

Linked Data

dbSNP Id: rs1359679486
gnomAD v3: 14-102573751-TA-T
gnomAD v4: 14-102573751-TA-T
MyVariant Identifiers: chr14:g.103040089del (hg19) chr14:g.102573752del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102573753del , CM000676.2:g.102573753del GRCh38
NC_000014.8:g.103040090del , CM000676.1:g.103040090del GRCh37
NC_000014.7:g.102109843del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944240.1:n.609-6334del
Search 100 bp 5'
Search 100 bp 3'