Canonical Allele Identifier: CA2608488239
Gene: MIR1915HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494708del , CM000672.2:g.21494708del GRCh38
NC_000010.10:g.21783637del , CM000672.1:g.21783637del GRCh37
NC_000010.9:g.21823643del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*895del ENSP00000366317.5:n.*895del
NM_001010911.2:c.*895del NP_001010911.1:n.*895del
NM_001010911.3:c.*895del NP_001010911.1:n.*895del
NR_160800.1:n.1752del