Canonical Allele Identifier: CA2153421497
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021358A= , CM000676.2:g.88021358A= GRCh38
NC_000014.8:g.88487702A= , CM000676.1:g.88487702A= GRCh37
NC_000014.7:g.87557455A= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2317T=