Canonical Allele Identifier: CA2703126796
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs2106893158

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124000C>T , CM000665.2:g.87124000C>T GRCh38
NC_000003.11:g.87173150C>T , CM000665.1:g.87173150C>T GRCh37
NC_000003.10:g.87255840C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30338C>T