Canonical Allele Identifier: CA471213813
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1312138975
gnomAD v2: 10-101287578-C-T
gnomAD v3: 10-99527821-C-T
gnomAD v4: 10-99527821-C-T
MyVariant Identifiers: chr10:g.101287578C>T (hg19) chr10:g.99527821C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527821C>T , CM000672.2:g.99527821C>T GRCh38
NC_000010.10:g.101287578C>T , CM000672.1:g.101287578C>T GRCh37
NC_000010.9:g.101277568C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.562G>A
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Search 100 bp 3'