ClinGen Allele Registry
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Canonical Allele Identifier:
CA2734039702
Gene: LINC00469
HGNC
NCBI
Linked Data
dbSNP Id:
rs2143599715
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.73811615G>A , CM000679.2:g.73811615G>A
GRCh38
NC_000017.10:g.71807754G>A , CM000679.1:g.71807754G>A
GRCh37
NC_000017.9:g.69319349G>A
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_027146.1:n.228+12073C>T
Search 100 bp 5'
Search 100 bp 3'