ClinGen Allele Registry
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Canonical Allele Identifier:
CA2274723138
Gene: LINC00469
HGNC
NCBI
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000017.11:g.73811575A= , CM000679.2:g.73811575A=
GRCh38
NC_000017.10:g.71807714A= , CM000679.1:g.71807714A=
GRCh37
NC_000017.9:g.69319309A=
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_027146.1:n.228+12113T=
Search 100 bp 5'
Search 100 bp 3'