Canonical Allele Identifier: CA1931371416
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528010T= , CM000672.2:g.99528010T= GRCh38
NC_000010.10:g.101287767T= , CM000672.1:g.101287767T= GRCh37
NC_000010.9:g.101277757T= NCBI36
NG_016854.1:g.78T=

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.373A=