Canonical Allele Identifier: CA1314064452
Gene: LINC01473 HGNC NCBI

Linked Data

dbSNP Id: rs1687733812

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079891G>A , CM000664.2:g.186079891G>A GRCh38
NC_000002.11:g.186944618G>A , CM000664.1:g.186944618G>A GRCh37
NC_000002.10:g.186652863G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1439C>T