Canonical Allele Identifier: CA1314064500
Gene: LINC01473 HGNC NCBI

Linked Data

dbSNP Id: rs1687735145

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186080001G>T , CM000664.2:g.186080001G>T GRCh38
NC_000002.11:g.186944728G>T , CM000664.1:g.186944728G>T GRCh37
NC_000002.10:g.186652973G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1329C>A