Canonical Allele Identifier: CA780892689
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1255832288
gnomAD v3: 18-5857233-G-T
gnomAD v4: 18-5857233-G-T
MyVariant Identifiers: chr18:g.5857232G>T (hg19) chr18:g.5857233G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5857233G>T , CM000680.2:g.5857233G>T GRCh38
NC_000018.9:g.5857232G>T , CM000680.1:g.5857232G>T GRCh37
NC_000018.8:g.5847232G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21210G>T
NR_172495.1:n.603-19020G>T
NR_172496.1:n.603-19020G>T
NR_172497.1:n.603-19020G>T
NR_172498.1:n.663-9880G>T
NR_172499.1:n.603-19020G>T
NR_172500.1:n.603-19020G>T
NR_172501.1:n.603-19020G>T
NR_172502.1:n.603-19020G>T
NR_172503.1:n.603-19020G>T
Search 100 bp 5'
Search 100 bp 3'