Canonical Allele Identifier: CA2282154389
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1468497239

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856966T>G , CM000680.2:g.5856966T>G GRCh38
NC_000018.9:g.5856965T>G , CM000680.1:g.5856965T>G GRCh37
NC_000018.8:g.5846965T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21477T>G
NR_172495.1:n.603-19287T>G
NR_172496.1:n.603-19287T>G
NR_172497.1:n.603-19287T>G
NR_172498.1:n.663-10147T>G
NR_172499.1:n.603-19287T>G
NR_172500.1:n.603-19287T>G
NR_172501.1:n.603-19287T>G
NR_172502.1:n.603-19287T>G
NR_172503.1:n.603-19287T>G