Canonical Allele Identifier: CA709662662
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1259465753

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021410C>T , CM000676.2:g.88021410C>T GRCh38
NC_000014.8:g.88487754C>T , CM000676.1:g.88487754C>T GRCh37
NC_000014.7:g.87557507C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110121.1:n.327+2265G>A