Canonical Allele Identifier: CA2153421438
Gene: LINC01147 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021307A= , CM000676.2:g.88021307A= GRCh38
NC_000014.8:g.88487651A= , CM000676.1:g.88487651A= GRCh37
NC_000014.7:g.87557404A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2368T=