Canonical Allele Identifier: CA471214131
Gene: LINC01475 HGNC NCBI

Linked Data

gnomAD v4: 10-99527930-G-T
MyVariant Identifiers: chr10:g.101287687G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527930G>T , CM000672.2:g.99527930G>T GRCh38
NC_000010.10:g.101287687G>T , CM000672.1:g.101287687G>T GRCh37
NC_000010.9:g.101277677G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.453C>A
Search 100 bp 5'
Search 100 bp 3'