Canonical Allele Identifier: CA471214367
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287768G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99528011G>T , CM000672.2:g.99528011G>T GRCh38
NC_000010.10:g.101287768G>T , CM000672.1:g.101287768G>T GRCh37
NC_000010.9:g.101277758G>T NCBI36
NG_016854.1:g.79G>T

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.372C>A