Canonical Allele Identifier: CA295688503

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs561613598
• gnomAD v3: 18-5856918-G-T
• gnomAD v4: 18-5856918-G-T
• MyVariant Identifiers: chr18:g.5856917G>T (hg19) ; chr18:g.5856918G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5856918G>T , CM000680.2:g.5856918G>T	GRCh38
NC_000018.9:g.5856917G>T , CM000680.1:g.5856917G>T	GRCh37
NC_000018.8:g.5846917G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_172494.1:n.603-21525G>T
NR_172495.1:n.603-19335G>T
NR_172496.1:n.603-19335G>T
NR_172497.1:n.603-19335G>T
NR_172498.1:n.663-10195G>T
NR_172499.1:n.603-19335G>T
NR_172500.1:n.603-19335G>T
NR_172501.1:n.603-19335G>T
NR_172502.1:n.603-19335G>T
NR_172503.1:n.603-19335G>T