Canonical Allele Identifier: CA1931371293
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527929T= , CM000672.2:g.99527929T= GRCh38
NC_000010.10:g.101287686T= , CM000672.1:g.101287686T= GRCh37
NC_000010.9:g.101277676T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.454A=