Canonical Allele Identifier: CA1895702168
Gene: MIR1915HG HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494721C= , CM000672.2:g.21494721C= GRCh38
NC_000010.10:g.21783650C= , CM000672.1:g.21783650C= GRCh37
NC_000010.9:g.21823656C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*879G= ENSP00000366317.5:n.*879G=
NM_001010911.2:c.*879G= NP_001010911.1:n.*879G=
NM_001010911.3:c.*879G= NP_001010911.1:n.*879G=
NR_160800.1:n.1736G=