Canonical Allele Identifier: CA295688497

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs201828028
• gnomAD v2: 18-5856906-C-A
• gnomAD v3: 18-5856907-C-A
• gnomAD v4: 18-5856907-C-A
• MyVariant Identifiers: chr18:g.5856906C>A (hg19) ; chr18:g.5856907C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5856907C>A , CM000680.2:g.5856907C>A	GRCh38
NC_000018.9:g.5856906C>A , CM000680.1:g.5856906C>A	GRCh37
NC_000018.8:g.5846906C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_172494.1:n.603-21536C>A
NR_172495.1:n.603-19346C>A
NR_172496.1:n.603-19346C>A
NR_172497.1:n.603-19346C>A
NR_172498.1:n.663-10206C>A
NR_172499.1:n.603-19346C>A
NR_172500.1:n.603-19346C>A
NR_172501.1:n.603-19346C>A
NR_172502.1:n.603-19346C>A
NR_172503.1:n.603-19346C>A