Canonical Allele Identifier: CA2802493887
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021267T>C , CM000676.2:g.88021267T>C GRCh38
NC_000014.8:g.88487611T>C , CM000676.1:g.88487611T>C GRCh37
NC_000014.7:g.87557364T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2408A>G