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Canonical Allele Identifier:
CA471214072
Gene: LINC01475
HGNC
NCBI
Linked Data
gnomAD v4:
10-99527910-A-C
MyVariant Identifiers:
chr10:g.101287667A>C (hg19)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000010.11:g.99527910A>C , CM000672.2:g.99527910A>C
GRCh38
NC_000010.10:g.101287667A>C , CM000672.1:g.101287667A>C
GRCh37
NC_000010.9:g.101277657A>C
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_120618.1:n.473T>G
Search 100 bp 5'
Search 100 bp 3'