Canonical Allele Identifier: CA1381485222
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs1704493137

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87123959C>G , CM000665.2:g.87123959C>G GRCh38
NC_000003.11:g.87173109C>G , CM000665.1:g.87173109C>G GRCh37
NC_000003.10:g.87255799C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_104153.1:n.329-30379C>G