Canonical Allele Identifier: CA1895702169
Gene: MIR1915HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494722G= , CM000672.2:g.21494722G= GRCh38
NC_000010.10:g.21783651G= , CM000672.1:g.21783651G= GRCh37
NC_000010.9:g.21823657G= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*878C= ENSP00000366317.5:n.*878C=
NM_001010911.2:c.*878C= NP_001010911.1:n.*878C=
NM_001010911.3:c.*878C= NP_001010911.1:n.*878C=
NR_160800.1:n.1735C=