Canonical Allele Identifier: CA1931371317
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527939A= , CM000672.2:g.99527939A= GRCh38
NC_000010.10:g.101287696A= , CM000672.1:g.101287696A= GRCh37
NC_000010.9:g.101277686A= NCBI36
NG_016854.1:g.7A=

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.444T=