Canonical Allele Identifier: CA965693551
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887827255

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021259T>C , CM000676.2:g.88021259T>C GRCh38
NC_000014.8:g.88487603T>C , CM000676.1:g.88487603T>C GRCh37
NC_000014.7:g.87557356T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2416A>G