Canonical Allele Identifier: CA2282154517

Gene: MIR3976HG

Linked Data

• dbSNP Id: rs2095145777

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.5857248A>C , CM000680.2:g.5857248A>C	GRCh38
NC_000018.9:g.5857247A>C , CM000680.1:g.5857247A>C	GRCh37
NC_000018.8:g.5847247A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NR_172494.1:n.603-21195A>C
NR_172495.1:n.603-19005A>C
NR_172496.1:n.603-19005A>C
NR_172497.1:n.603-19005A>C
NR_172498.1:n.663-9865A>C
NR_172499.1:n.603-19005A>C
NR_172500.1:n.603-19005A>C
NR_172501.1:n.603-19005A>C
NR_172502.1:n.603-19005A>C
NR_172503.1:n.603-19005A>C