Canonical Allele Identifier: CA2153421379
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887827144

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021254G>A , CM000676.2:g.88021254G>A GRCh38
NC_000014.8:g.88487598G>A , CM000676.1:g.88487598G>A GRCh37
NC_000014.7:g.87557351G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2421C>T