Canonical Allele Identifier: CA2282154359
Gene: MIR3976HG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.5856912_5856913delinsCT , CM000680.2:g.5856912_5856913delinsCT GRCh38
NC_000018.9:g.5856911_5856912delinsCT , CM000680.1:g.5856911_5856912delinsCT GRCh37
NC_000018.8:g.5846911_5846912delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_172494.1:n.603-21531_603-21530delinsCT
NR_172495.1:n.603-19341_603-19340delinsCT
NR_172496.1:n.603-19341_603-19340delinsCT
NR_172497.1:n.603-19341_603-19340delinsCT
NR_172498.1:n.663-10201_663-10200delinsCT
NR_172499.1:n.603-19341_603-19340delinsCT
NR_172500.1:n.603-19341_603-19340delinsCT
NR_172501.1:n.603-19341_603-19340delinsCT
NR_172502.1:n.603-19341_603-19340delinsCT
NR_172503.1:n.603-19341_603-19340delinsCT
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