Canonical Allele Identifier: CA2153421401
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021271G= , CM000676.2:g.88021271G= GRCh38
NC_000014.8:g.88487615G= , CM000676.1:g.88487615G= GRCh37
NC_000014.7:g.87557368G= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2404C=