Canonical Allele Identifier: CA1931371081
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527815C= , CM000672.2:g.99527815C= GRCh38
NC_000010.10:g.101287572C= , CM000672.1:g.101287572C= GRCh37
NC_000010.9:g.101277562C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.568G=