Canonical Allele Identifier: CA471213895
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1186958887

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527850A>C , CM000672.2:g.99527850A>C GRCh38
NC_000010.10:g.101287607A>C , CM000672.1:g.101287607A>C GRCh37
NC_000010.9:g.101277597A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.533T>G