Canonical Allele Identifier: CA62498367
Gene: LINC01473 HGNC NCBI

Linked Data

dbSNP Id: rs1024360646

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079973G>A , CM000664.2:g.186079973G>A GRCh38
NC_000002.11:g.186944700G>A , CM000664.1:g.186944700G>A GRCh37
NC_000002.10:g.186652945G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1357C>T