Canonical Allele Identifier: CA965693581
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887827776

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021286C>A , CM000676.2:g.88021286C>A GRCh38
NC_000014.8:g.88487630C>A , CM000676.1:g.88487630C>A GRCh37
NC_000014.7:g.87557383C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2389G>T