Canonical Allele Identifier: CA295688507
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1001000110
gnomAD v3: 18-5856936-C-T
gnomAD v4: 18-5856936-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856936C>T , CM000680.2:g.5856936C>T GRCh38
NC_000018.9:g.5856935C>T , CM000680.1:g.5856935C>T GRCh37
NC_000018.8:g.5846935C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_172494.1:n.603-21507C>T
NR_172495.1:n.603-19317C>T
NR_172496.1:n.603-19317C>T
NR_172497.1:n.603-19317C>T
NR_172498.1:n.663-10177C>T
NR_172499.1:n.603-19317C>T
NR_172500.1:n.603-19317C>T
NR_172501.1:n.603-19317C>T
NR_172502.1:n.603-19317C>T
NR_172503.1:n.603-19317C>T