Canonical Allele Identifier: CA79020298
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs987633826
gnomAD v3: 3-87124030-C-A
gnomAD v4: 3-87124030-C-A
MyVariant Identifiers: chr3:g.87173180C>A (hg19) chr3:g.87124030C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124030C>A , CM000665.2:g.87124030C>A GRCh38
NC_000003.11:g.87173180C>A , CM000665.1:g.87173180C>A GRCh37
NC_000003.10:g.87255870C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30308C>A
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Search 100 bp 3'