Canonical Allele Identifier: CA295688504
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs888773175
gnomAD v3: 18-5856920-A-G
gnomAD v4: 18-5856920-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856920A>G , CM000680.2:g.5856920A>G GRCh38
NC_000018.9:g.5856919A>G , CM000680.1:g.5856919A>G GRCh37
NC_000018.8:g.5846919A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21523A>G
NR_172495.1:n.603-19333A>G
NR_172496.1:n.603-19333A>G
NR_172497.1:n.603-19333A>G
NR_172498.1:n.663-10193A>G
NR_172499.1:n.603-19333A>G
NR_172500.1:n.603-19333A>G
NR_172501.1:n.603-19333A>G
NR_172502.1:n.603-19333A>G
NR_172503.1:n.603-19333A>G