Canonical Allele Identifier: CA471214160
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287697C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527940C>T , CM000672.2:g.99527940C>T GRCh38
NC_000010.10:g.101287697C>T , CM000672.1:g.101287697C>T GRCh37
NC_000010.9:g.101277687C>T NCBI36
NG_016854.1:g.8C>T

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.443G>A