Canonical Allele Identifier: CA911624723
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1328089774
gnomAD v3: 3-87124096-T-C
gnomAD v4: 3-87124096-T-C
MyVariant Identifiers: chr3:g.87173246T>C (hg19) chr3:g.87124096T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124096T>C , CM000665.2:g.87124096T>C GRCh38
NC_000003.11:g.87173246T>C , CM000665.1:g.87173246T>C GRCh37
NC_000003.10:g.87255936T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30242T>C
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Search 100 bp 3'