Canonical Allele Identifier: CA2282154395
Gene: MIR3976HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856973T= , CM000680.2:g.5856973T= GRCh38
NC_000018.9:g.5856972T= , CM000680.1:g.5856972T= GRCh37
NC_000018.8:g.5846972T= NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21470T=
NR_172495.1:n.603-19280T=
NR_172496.1:n.603-19280T=
NR_172497.1:n.603-19280T=
NR_172498.1:n.663-10140T=
NR_172499.1:n.603-19280T=
NR_172500.1:n.603-19280T=
NR_172501.1:n.603-19280T=
NR_172502.1:n.603-19280T=
NR_172503.1:n.603-19280T=