Canonical Allele Identifier: CA2282154468
Gene: MIR3976HG HGNC NCBI

Linked Data

dbSNP Id: rs2095145708

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5857127_5857129del , CM000680.2:g.5857127_5857129del GRCh38
NC_000018.9:g.5857126_5857128del , CM000680.1:g.5857126_5857128del GRCh37
NC_000018.8:g.5847126_5847128del NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21316_603-21314del
NR_172495.1:n.603-19126_603-19124del
NR_172496.1:n.603-19126_603-19124del
NR_172497.1:n.603-19126_603-19124del
NR_172498.1:n.663-9986_663-9984del
NR_172499.1:n.603-19126_603-19124del
NR_172500.1:n.603-19126_603-19124del
NR_172501.1:n.603-19126_603-19124del
NR_172502.1:n.603-19126_603-19124del
NR_172503.1:n.603-19126_603-19124del