Canonical Allele Identifier: CA2153421390
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021259T= , CM000676.2:g.88021259T= GRCh38
NC_000014.8:g.88487603T= , CM000676.1:g.88487603T= GRCh37
NC_000014.7:g.87557356T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2416A=