Canonical Allele Identifier: CA2153421538
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887829813

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021384T>G , CM000676.2:g.88021384T>G GRCh38
NC_000014.8:g.88487728T>G , CM000676.1:g.88487728T>G GRCh37
NC_000014.7:g.87557481T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2291A>C