Canonical Allele Identifier: CA2282154367
Gene: MIR3976HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856925T= , CM000680.2:g.5856925T= GRCh38
NC_000018.9:g.5856924T= , CM000680.1:g.5856924T= GRCh37
NC_000018.8:g.5846924T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21518T=
NR_172495.1:n.603-19328T=
NR_172496.1:n.603-19328T=
NR_172497.1:n.603-19328T=
NR_172498.1:n.663-10188T=
NR_172499.1:n.603-19328T=
NR_172500.1:n.603-19328T=
NR_172501.1:n.603-19328T=
NR_172502.1:n.603-19328T=
NR_172503.1:n.603-19328T=