Canonical Allele Identifier: CA471214380
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287773A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528016A>T , CM000672.2:g.99528016A>T GRCh38
NC_000010.10:g.101287773A>T , CM000672.1:g.101287773A>T GRCh37
NC_000010.9:g.101277763A>T NCBI36
NG_016854.1:g.84A>T

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.367T>A