Canonical Allele Identifier: CA471214158
Gene: LINC01475 HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.101287697C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527940C>A , CM000672.2:g.99527940C>A GRCh38
NC_000010.10:g.101287697C>A , CM000672.1:g.101287697C>A GRCh37
NC_000010.9:g.101277687C>A NCBI36
NG_016854.1:g.8C>A

Transcript Alleles

HGVS Amino-acid change
NR_120618.1:n.443G>T
Search 100 bp 5'
Search 100 bp 3'