Canonical Allele Identifier: CA628100796
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs1485846086

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856997del , CM000680.2:g.5856997del GRCh38
NC_000018.9:g.5856996del , CM000680.1:g.5856996del GRCh37
NC_000018.8:g.5846996del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21446del
NR_172495.1:n.603-19256del
NR_172496.1:n.603-19256del
NR_172497.1:n.603-19256del
NR_172498.1:n.663-10116del
NR_172499.1:n.603-19256del
NR_172500.1:n.603-19256del
NR_172501.1:n.603-19256del
NR_172502.1:n.603-19256del
NR_172503.1:n.603-19256del