Canonical Allele Identifier: CA2802493884
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021173A>G , CM000676.2:g.88021173A>G GRCh38
NC_000014.8:g.88487517A>G , CM000676.1:g.88487517A>G GRCh37
NC_000014.7:g.87557270A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.328-2470T>C