Canonical Allele Identifier: CA2153421342
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021222T= , CM000676.2:g.88021222T= GRCh38
NC_000014.8:g.88487566T= , CM000676.1:g.88487566T= GRCh37
NC_000014.7:g.87557319T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2453A=