Canonical Allele Identifier: CA780892581
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1468497239
gnomAD v3: 18-5856966-T-A
gnomAD v4: 18-5856966-T-A
MyVariant Identifiers: chr18:g.5856965T>A (hg19) chr18:g.5856966T>A (hg38)
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Genomic Alleles

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

Transcript Alleles

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