Canonical Allele Identifier: CA2282154509
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs2095145768

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5857231A>G , CM000680.2:g.5857231A>G GRCh38
NC_000018.9:g.5857230A>G , CM000680.1:g.5857230A>G GRCh37
NC_000018.8:g.5847230A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21212A>G
NR_172495.1:n.603-19022A>G
NR_172496.1:n.603-19022A>G
NR_172497.1:n.603-19022A>G
NR_172498.1:n.663-9882A>G
NR_172499.1:n.603-19022A>G
NR_172500.1:n.603-19022A>G
NR_172501.1:n.603-19022A>G
NR_172502.1:n.603-19022A>G
NR_172503.1:n.603-19022A>G