Canonical Allele Identifier: CA911624731
Gene: LINC00506 HGNC NCBI

Linked Data

dbSNP Id: rs906250859

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.87124121A>C , CM000665.2:g.87124121A>C GRCh38
NC_000003.11:g.87173271A>C , CM000665.1:g.87173271A>C GRCh37
NC_000003.10:g.87255961A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_104153.1:n.329-30217A>C