Canonical Allele Identifier: CA471214109
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287679T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527922T>G , CM000672.2:g.99527922T>G GRCh38
NC_000010.10:g.101287679T>G , CM000672.1:g.101287679T>G GRCh37
NC_000010.9:g.101277669T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.461A>C