Canonical Allele Identifier: CA2282154375
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1599513877
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856938T>A , CM000680.2:g.5856938T>A GRCh38
NC_000018.9:g.5856937T>A , CM000680.1:g.5856937T>A GRCh37
NC_000018.8:g.5846937T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21505T>A
NR_172495.1:n.603-19315T>A
NR_172496.1:n.603-19315T>A
NR_172497.1:n.603-19315T>A
NR_172498.1:n.663-10175T>A
NR_172499.1:n.603-19315T>A
NR_172500.1:n.603-19315T>A
NR_172501.1:n.603-19315T>A
NR_172502.1:n.603-19315T>A
NR_172503.1:n.603-19315T>A
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