Canonical Allele Identifier: CA911624671
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1418763814
MyVariant Identifiers: chr3:g.87173162A>G (hg19) chr3:g.87124012A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124012A>G , CM000665.2:g.87124012A>G GRCh38
NC_000003.11:g.87173162A>G , CM000665.1:g.87173162A>G GRCh37
NC_000003.10:g.87255852A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30326A>G
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