ClinGen Allele Registry
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Canonical Allele Identifier:
CA127211580
Gene: MIR3936HG
HGNC
NCBI
Linked Data
dbSNP Id:
rs923192893
gnomAD v3:
5-132350399-C-T
gnomAD v4:
5-132350399-C-T
MyVariant Identifiers:
chr5:g.131686092C>T (hg19)
chr5:g.132350399C>T (hg38)
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.132350399C>T , CM000667.2:g.132350399C>T
GRCh38
NC_000005.9:g.131686092C>T , CM000667.1:g.131686092C>T
GRCh37
NC_000005.8:g.131713991C>T
NCBI36
Transcript Alleles
HGVS
Amino-acid change
NR_110997.1:n.418-442G>A
Search 100 bp 5'
Search 100 bp 3'