Canonical Allele Identifier: CA1381485602
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1704496959

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124236A>C , CM000665.2:g.87124236A>C GRCh38
NC_000003.11:g.87173386A>C , CM000665.1:g.87173386A>C GRCh37
NC_000003.10:g.87256076A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30102A>C