Canonical Allele Identifier: CA2802493892
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021427G>T , CM000676.2:g.88021427G>T GRCh38
NC_000014.8:g.88487771G>T , CM000676.1:g.88487771G>T GRCh37
NC_000014.7:g.87557524G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2248C>A