Canonical Allele Identifier: CA1931371250
Gene: LINC01475 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527915A= , CM000672.2:g.99527915A= GRCh38
NC_000010.10:g.101287672A= , CM000672.1:g.101287672A= GRCh37
NC_000010.9:g.101277662A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.468T=