ClinGen Allele Registry
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Canonical Allele Identifier:
CA989994777
Gene: MIR4527HG
HGNC
NCBI
Linked Data - Sequence & Population
gnomAD v3:
18:47333893 G / C
gnomAD v4:
chr18-47333893-G-C
Linked Data - NCBI & NCI
dbSNP:
9947662
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000018.10:g.47333893G>C , CM000680.2:g.47333893G>C
GRCh38
NC_000018.9:g.44860264G>C , CM000680.1:g.44860264G>C
GRCh37
NC_000018.8:g.43114262G>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_147192.1:n.38+48132G>C
Search 100 bp 5'
Search 100 bp 3'