Canonical Allele Identifier: CA1895702163
Gene: MIR1915HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494713T= , CM000672.2:g.21494713T= GRCh38
NC_000010.10:g.21783642T= , CM000672.1:g.21783642T= GRCh37
NC_000010.9:g.21823648T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*887A= ENSP00000366317.5:n.*887A=
NM_001010911.2:c.*887A= NP_001010911.1:n.*887A=
NM_001010911.3:c.*887A= NP_001010911.1:n.*887A=
NR_160800.1:n.1744A=