Canonical Allele Identifier: CA267344123
Gene: LINC02323 HGNC NCBI

Linked Data

dbSNP Id: rs928450801
gnomAD v3: 14-102573746-CTATT-C
gnomAD v4: 14-102573746-CTATT-C
MyVariant Identifiers: chr14:g.103040084_103040087del (hg19) chr14:g.102573747_102573750del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.102573749_102573752del , CM000676.2:g.102573749_102573752del GRCh38
NC_000014.8:g.103040086_103040089del , CM000676.1:g.103040086_103040089del GRCh37
NC_000014.7:g.102109839_102109842del NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_944240.1:n.609-6338_609-6335del
Search 100 bp 5'
Search 100 bp 3'