Canonical Allele Identifier: CA1381485260
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1575928623
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Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124017T>C , CM000665.2:g.87124017T>C GRCh38
NC_000003.11:g.87173167T>C , CM000665.1:g.87173167T>C GRCh37
NC_000003.10:g.87255857T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30321T>C
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