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Canonical Allele Identifier:
CA15373588
Gene: MIR3936HG
HGNC
NCBI
Linked Data - Predicted Effect Evidence
MyVariant.info:
GRCh38
chr5:g.132364175A>G
GRCh37
chr5:g.131699867A>G
Linked Data - Sequence & Population
gnomAD v2:
5:131699867 A / G
gnomAD v3:
5:132364175 A / G
gnomAD v4:
chr5-132364175-A-G
Joint Max Group AF
0.72579029 (AFR)
Genomes Max Group AF
0.72579029 (AFR)
Linked Data - NCBI & NCI
dbSNP:
274546
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.132364175A>G , CM000667.2:g.132364175A>G
GRCh38
NC_000005.9:g.131699867A>G , CM000667.1:g.131699867A>G
GRCh37
NC_000005.8:g.131727766A>G
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_110997.1:n.380+760T>C
Search 100 bp 5'
Search 100 bp 3'