Canonical Allele Identifier: CA265472411
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs368121194
gnomAD v2: 14-88487650-T-G
gnomAD v3: 14-88021306-T-G
gnomAD v4: 14-88021306-T-G
MyVariant Identifiers: chr14:g.88487650T>G (hg19) chr14:g.88021306T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021306T>G , CM000676.2:g.88021306T>G GRCh38
NC_000014.8:g.88487650T>G , CM000676.1:g.88487650T>G GRCh37
NC_000014.7:g.87557403T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2369A>C
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