Canonical Allele Identifier: CA1931370918
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527713A= , CM000672.2:g.99527713A= GRCh38
NC_000010.10:g.101287470A= , CM000672.1:g.101287470A= GRCh37
NC_000010.9:g.101277460A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.577+93T=