Canonical Allele Identifier: CA965693499
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1887825964
gnomAD v3: 14-88021171-C-T
gnomAD v4: 14-88021171-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021171C>T , CM000676.2:g.88021171C>T GRCh38
NC_000014.8:g.88487515C>T , CM000676.1:g.88487515C>T GRCh37
NC_000014.7:g.87557268C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.328-2468G>A
Search 100 bp 5'
Search 100 bp 3'