Canonical Allele Identifier: CA213043629
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs544501526
gnomAD v2: 10-101288860-C-T
gnomAD v3: 10-99529103-C-T
gnomAD v4: 10-99529103-C-T
MyVariant Identifiers: chr10:g.101288860C>T (hg19) chr10:g.99529103C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99529103C>T , CM000672.2:g.99529103C>T GRCh38
NC_000010.10:g.101288860C>T , CM000672.1:g.101288860C>T GRCh37
NC_000010.9:g.101278850C>T NCBI36
NG_016854.1:g.1171C>T

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.167-419G>A
Search 100 bp 5'
Search 100 bp 3'