Canonical Allele Identifier: CA127211589
Gene: MIR3936HG HGNC NCBI
dbSNP:
10058074
gnomAD v2:
5:131686146 G / A
gnomAD v3:
5:132350453 G / A
gnomAD v4:
chr5-132350453-G-A
Joint Max Group AF 0.45332112 (NFE)
Genomes Max Group AF 0.45332112 (NFE)
MyVariant.info:
GRCh38 chr5:g.132350453G>A
GRCh37 chr5:g.131686146G>A
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.132350453G>A , CM000667.2:g.132350453G>A GRCh38
NC_000005.9:g.131686146G>A , CM000667.1:g.131686146G>A GRCh37
NC_000005.8:g.131714045G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110997.1:n.418-496C>T
Search 100 bp 5'
Search 100 bp 3'