Canonical Allele Identifier: CA1592062058
Gene: LINC01470 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.152908893T>A , CM000667.2:g.152908893T>A GRCh38
NC_000005.9:g.152288453T>A , CM000667.1:g.152288453T>A GRCh37
NC_000005.8:g.152268646T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_109877.1:n.178+57348A>T