Canonical Allele Identifier: CA471213868
Gene: LINC01475 HGNC NCBI

Linked Data

gnomAD v4: 10-99527841-A-C
MyVariant Identifiers: chr10:g.101287598A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527841A>C , CM000672.2:g.99527841A>C GRCh38
NC_000010.10:g.101287598A>C , CM000672.1:g.101287598A>C GRCh37
NC_000010.9:g.101277588A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.542T>G
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