Canonical Allele Identifier: CA295688505

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs529642097
• gnomAD v2: 18-5856921-T-A
• gnomAD v3: 18-5856922-T-A
• gnomAD v4: 18-5856922-T-A
• MyVariant Identifiers: chr18:g.5856921T>A (hg19) ; chr18:g.5856922T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5856922T>A , CM000680.2:g.5856922T>A	GRCh38
NC_000018.9:g.5856921T>A , CM000680.1:g.5856921T>A	GRCh37
NC_000018.8:g.5846921T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_172494.1:n.603-21521T>A
NR_172495.1:n.603-19331T>A
NR_172496.1:n.603-19331T>A
NR_172497.1:n.603-19331T>A
NR_172498.1:n.663-10191T>A
NR_172499.1:n.603-19331T>A
NR_172500.1:n.603-19331T>A
NR_172501.1:n.603-19331T>A
NR_172502.1:n.603-19331T>A
NR_172503.1:n.603-19331T>A