Canonical Allele Identifier: CA79020288
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs562122572
gnomAD v3: 3-87123907-C-T
gnomAD v4: 3-87123907-C-T
MyVariant Identifiers: chr3:g.87173057C>T (hg19) chr3:g.87123907C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87123907C>T , CM000665.2:g.87123907C>T GRCh38
NC_000003.11:g.87173057C>T , CM000665.1:g.87173057C>T GRCh37
NC_000003.10:g.87255747C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30431C>T
Search 100 bp 5'
Search 100 bp 3'