Canonical Allele Identifier: CA931728657
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs569201373
gnomAD v3: 10-99529093-C-A
gnomAD v4: 10-99529093-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99529093C>A , CM000672.2:g.99529093C>A GRCh38
NC_000010.10:g.101288850C>A , CM000672.1:g.101288850C>A GRCh37
NC_000010.9:g.101278840C>A NCBI36
NG_016854.1:g.1161C>A

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.167-409G>T
Search 100 bp 5'
Search 100 bp 3'