Canonical Allele Identifier: CA1931375097
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99530606G= , CM000672.2:g.99530606G= GRCh38
NC_000010.10:g.101290363G= , CM000672.1:g.101290363G= GRCh37
NC_000010.9:g.101280353G= NCBI36
NG_016854.1:g.2674G=

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.166+406C=