Canonical Allele Identifier: CA1931375015
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99530544T= , CM000672.2:g.99530544T= GRCh38
NC_000010.10:g.101290301T= , CM000672.1:g.101290301T= GRCh37
NC_000010.9:g.101280291T= NCBI36
NG_016854.1:g.2612T=

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.166+468A=