Canonical Allele Identifier: CA1314064488
Gene: LINC01473 HGNC NCBI

Linked Data

dbSNP Id: rs1447464021

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079960T>A , CM000664.2:g.186079960T>A GRCh38
NC_000002.11:g.186944687T>A , CM000664.1:g.186944687T>A GRCh37
NC_000002.10:g.186652932T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1370A>T