Canonical Allele Identifier: CA1592062059
Gene: LINC01470 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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