Canonical Allele Identifier: CA265472425
Gene: LINC01147 HGNC NCBI

Linked Data

dbSNP Id: rs1028322017
gnomAD v2: 14-88487745-A-G
gnomAD v3: 14-88021401-A-G
gnomAD v4: 14-88021401-A-G
MyVariant Identifiers: chr14:g.88487745A>G (hg19) chr14:g.88021401A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.88021401A>G , CM000676.2:g.88021401A>G GRCh38
NC_000014.8:g.88487745A>G , CM000676.1:g.88487745A>G GRCh37
NC_000014.7:g.87557498A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110121.1:n.327+2274T>C
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