Canonical Allele Identifier: CA1931371449
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528019G= , CM000672.2:g.99528019G= GRCh38
NC_000010.10:g.101287776G= , CM000672.1:g.101287776G= GRCh37
NC_000010.9:g.101277766G= NCBI36
NG_016854.1:g.87G=

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.364C=