Canonical Allele Identifier: CA628100805

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs901576586
• gnomAD v2: 18-5857026-A-C
• gnomAD v3: 18-5857027-A-C
• gnomAD v4: 18-5857027-A-C
• MyVariant Identifiers: chr18:g.5857026A>C (hg19) ; chr18:g.5857027A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5857027A>C , CM000680.2:g.5857027A>C	GRCh38
NC_000018.9:g.5857026A>C , CM000680.1:g.5857026A>C	GRCh37
NC_000018.8:g.5847026A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
NR_172494.1:n.603-21416A>C
NR_172495.1:n.603-19226A>C
NR_172496.1:n.603-19226A>C
NR_172497.1:n.603-19226A>C
NR_172498.1:n.663-10086A>C
NR_172499.1:n.603-19226A>C
NR_172500.1:n.603-19226A>C
NR_172501.1:n.603-19226A>C
NR_172502.1:n.603-19226A>C
NR_172503.1:n.603-19226A>C