Canonical Allele Identifier: CA471214155
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1337374865
gnomAD v2: 10-101287696-A-T
gnomAD v3: 10-99527939-A-T
gnomAD v4: 10-99527939-A-T
MyVariant Identifiers: chr10:g.101287696A>T (hg19) chr10:g.99527939A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527939A>T , CM000672.2:g.99527939A>T GRCh38
NC_000010.10:g.101287696A>T , CM000672.1:g.101287696A>T GRCh37
NC_000010.9:g.101277686A>T NCBI36
NG_016854.1:g.7A>T

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.444T>A
Search 100 bp 5'
Search 100 bp 3'