Canonical Allele Identifier: CA2734586145
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs2144362447
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5857110T>A , CM000680.2:g.5857110T>A GRCh38
NC_000018.9:g.5857109T>A , CM000680.1:g.5857109T>A GRCh37
NC_000018.8:g.5847109T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21333T>A
NR_172495.1:n.603-19143T>A
NR_172496.1:n.603-19143T>A
NR_172497.1:n.603-19143T>A
NR_172498.1:n.663-10003T>A
NR_172499.1:n.603-19143T>A
NR_172500.1:n.603-19143T>A
NR_172501.1:n.603-19143T>A
NR_172502.1:n.603-19143T>A
NR_172503.1:n.603-19143T>A
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