Canonical Allele Identifier: CA670599805
Gene: LINC01475 HGNC NCBI

Linked Data

dbSNP Id: rs1379383645
gnomAD v4: 10-99527773-G-A
MyVariant Identifiers: chr10:g.101287530G>A (hg19) chr10:g.99527773G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.99527773G>A , CM000672.2:g.99527773G>A GRCh38
NC_000010.10:g.101287530G>A , CM000672.1:g.101287530G>A GRCh37
NC_000010.9:g.101277520G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_120618.1:n.577+33C>T
Search 100 bp 5'
Search 100 bp 3'