Canonical Allele Identifier: CA471213874
Gene: LINC01475 HGNC NCBI

Linked Data

gnomAD v4: 10-99527843-C-A
MyVariant Identifiers: chr10:g.101287600C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527843C>A , CM000672.2:g.99527843C>A GRCh38
NC_000010.10:g.101287600C>A , CM000672.1:g.101287600C>A GRCh37
NC_000010.9:g.101277590C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.540G>T
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