Canonical Allele Identifier: CA252769210
Gene: LINC00347 HGNC NCBI

Linked Data

dbSNP Id: rs17718828

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.74553977C>T , CM000675.2:g.74553977C>T GRCh38
NC_000013.10:g.75128114C>T , CM000675.1:g.75128114C>T GRCh37
NC_000013.9:g.74026115C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_034024.1:n.62-636C>T
NR_034025.1:n.62-680C>T