Canonical Allele Identifier: CA535050366
Gene: LINC01104 HGNC NCBI

Linked Data

dbSNP Id: rs1457502428
gnomAD v2: 2-100835611-G-A
gnomAD v3: 2-100219149-G-A
gnomAD v4: 2-100219149-G-A
MyVariant Identifiers: chr2:g.100835611G>A (hg19) chr2:g.100219149G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.100219149G>A , CM000664.2:g.100219149G>A GRCh38
NC_000002.11:g.100835611G>A , CM000664.1:g.100835611G>A GRCh37
NC_000002.10:g.100202043G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_103730.1:n.567+10329G>A
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