Canonical Allele Identifier: CA471213840
Gene: LINC01475 HGNC NCBI

Linked Data

gnomAD v4: 10-99527831-G-T
MyVariant Identifiers: chr10:g.101287588G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527831G>T , CM000672.2:g.99527831G>T GRCh38
NC_000010.10:g.101287588G>T , CM000672.1:g.101287588G>T GRCh37
NC_000010.9:g.101277578G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.552C>A
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