Canonical Allele Identifier: CA987452992

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs2095145613
• gnomAD v3: 18-5856944-A-C
• gnomAD v4: 18-5856944-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5856944A>C , CM000680.2:g.5856944A>C	GRCh38
NC_000018.9:g.5856943A>C , CM000680.1:g.5856943A>C	GRCh37
NC_000018.8:g.5846943A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_172494.1:n.603-21499A>C
NR_172495.1:n.603-19309A>C
NR_172496.1:n.603-19309A>C
NR_172497.1:n.603-19309A>C
NR_172498.1:n.663-10169A>C
NR_172499.1:n.603-19309A>C
NR_172500.1:n.603-19309A>C
NR_172501.1:n.603-19309A>C
NR_172502.1:n.603-19309A>C
NR_172503.1:n.603-19309A>C