Canonical Allele Identifier: CA707221951
Gene: LINC01500 HGNC NCBI

Linked Data

dbSNP Id: rs1233068921
gnomAD v3: 14-58867432-CT-C
gnomAD v4: 14-58867432-CT-C
MyVariant Identifiers: chr14:g.59334151del (hg19) chr14:g.58867433del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.58867433del , CM000676.2:g.58867433del GRCh38
NC_000014.8:g.59334151del , CM000676.1:g.59334151del GRCh37
NC_000014.7:g.58403904del NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110547.1:n.269-26710del
Search 100 bp 5'
Search 100 bp 3'