Canonical Allele Identifier: CA965693589
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1172248064

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021311C>T , CM000676.2:g.88021311C>T GRCh38
NC_000014.8:g.88487655C>T , CM000676.1:g.88487655C>T GRCh37
NC_000014.7:g.87557408C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2364G>A