Canonical Allele Identifier: CA295688516
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs988224156
gnomAD v2: 18-5856967-C-T
gnomAD v3: 18-5856968-C-T
gnomAD v4: 18-5856968-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856968C>T , CM000680.2:g.5856968C>T GRCh38
NC_000018.9:g.5856967C>T , CM000680.1:g.5856967C>T GRCh37
NC_000018.8:g.5846967C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21475C>T
NR_172495.1:n.603-19285C>T
NR_172496.1:n.603-19285C>T
NR_172497.1:n.603-19285C>T
NR_172498.1:n.663-10145C>T
NR_172499.1:n.603-19285C>T
NR_172500.1:n.603-19285C>T
NR_172501.1:n.603-19285C>T
NR_172502.1:n.603-19285C>T
NR_172503.1:n.603-19285C>T