Canonical Allele Identifier: CA2153421564
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021401A= , CM000676.2:g.88021401A= GRCh38
NC_000014.8:g.88487745A= , CM000676.1:g.88487745A= GRCh37
NC_000014.7:g.87557498A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2274T=