Canonical Allele Identifier: CA1381485198
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1704492946

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87123930A>G , CM000665.2:g.87123930A>G GRCh38
NC_000003.11:g.87173080A>G , CM000665.1:g.87173080A>G GRCh37
NC_000003.10:g.87255770A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30408A>G