Canonical Allele Identifier: CA2701037912
Gene: LINC01473 HGNC NCBI

Linked Data

dbSNP Id: rs1185165944

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079964C>T , CM000664.2:g.186079964C>T GRCh38
NC_000002.11:g.186944691C>T , CM000664.1:g.186944691C>T GRCh37
NC_000002.10:g.186652936C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1366G>A