Canonical Allele Identifier: CA1895702099
Gene: MIR1915HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494609C= , CM000672.2:g.21494609C= GRCh38
NC_000010.10:g.21783538C= , CM000672.1:g.21783538C= GRCh37
NC_000010.9:g.21823544C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000377113.5:c.*991G= ENSP00000366317.5:n.*991G=
NM_001010911.2:c.*991G= NP_001010911.1:n.*991G=
NM_001010911.3:c.*991G= NP_001010911.1:n.*991G=
NR_160800.1:n.1848G=