Canonical Allele Identifier: CA965693618
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887829897

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021389G>A , CM000676.2:g.88021389G>A GRCh38
NC_000014.8:g.88487733G>A , CM000676.1:g.88487733G>A GRCh37
NC_000014.7:g.87557486G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2286C>T