Canonical Allele Identifier: CA1334817848
Gene: LINC00471 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.231513520T= , CM000664.2:g.231513520T= GRCh38
NC_000002.11:g.232378231T= , CM000664.1:g.232378231T= GRCh37
NC_000002.10:g.232086475T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_024079.1:n.364+7A=