Canonical Allele Identifier: CA471214111
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1454525179

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527923T>G , CM000672.2:g.99527923T>G GRCh38
NC_000010.10:g.101287680T>G , CM000672.1:g.101287680T>G GRCh37
NC_000010.9:g.101277670T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.460A>C