Canonical Allele Identifier: CA780892668
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1440024311
MyVariant Identifiers: chr18:g.5857110A>G (hg19) chr18:g.5857111A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5857111A>G , CM000680.2:g.5857111A>G GRCh38
NC_000018.9:g.5857110A>G , CM000680.1:g.5857110A>G GRCh37
NC_000018.8:g.5847110A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21332A>G
NR_172495.1:n.603-19142A>G
NR_172496.1:n.603-19142A>G
NR_172497.1:n.603-19142A>G
NR_172498.1:n.663-10002A>G
NR_172499.1:n.603-19142A>G
NR_172500.1:n.603-19142A>G
NR_172501.1:n.603-19142A>G
NR_172502.1:n.603-19142A>G
NR_172503.1:n.603-19142A>G
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