Canonical Allele Identifier: CA2608488240
Gene: MIR1915HG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.21494706G>T , CM000672.2:g.21494706G>T GRCh38
NC_000010.10:g.21783635G>T , CM000672.1:g.21783635G>T GRCh37
NC_000010.9:g.21823641G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000377113.5:c.*894C>A ENSP00000366317.5:n.*894C>A
NM_001010911.2:c.*894C>A NP_001010911.1:n.*894C>A
NM_001010911.3:c.*894C>A NP_001010911.1:n.*894C>A
NR_160800.1:n.1751C>A