Canonical Allele Identifier: CA471214390
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287777T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528020T>A , CM000672.2:g.99528020T>A GRCh38
NC_000010.10:g.101287777T>A , CM000672.1:g.101287777T>A GRCh37
NC_000010.9:g.101277767T>A NCBI36
NG_016854.1:g.88T>A

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.363A>T